esv3975639

Organism: Homo sapiens

Study:estd229 (Fakhro et al. 2015)
Variant Type:copy number variation
Method Type:SNP array, Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:59
Validation:Not tested
Clinical Assertions: No
Region Size:109,284

Publication(s):Fakhro et al. 2015

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 1073 SVs from 88 studies. See in: genome view

Remapped(Score: Good):418,161-527,444

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Stop	Outer Stop
esv3975639	Remapped	Good	GRCh38.p12	ALT_REF_LOCI_1	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	418,161	527,444	-
esv3975639	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	2,182,951	-	2,297,700

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Copy number	Other Calls in this Sample and Study
essv25962657	duplication	DGMQ-31497	SNP array, Sequencing	Other, Probe signal intensity, Read depth	4	1,530
essv25951601	duplication	DGMQ-32056	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,667
essv25995349	duplication	DGMQ-31529	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,515
essv26011107	duplication	DGMQ-31601	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,666
essv26026554	duplication	DGMQ-31582	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,592
essv26042360	duplication	DGMQ-31574	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,528
essv26045736	duplication	DGMQ-31514	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,529
essv25910359	duplication	DGMQ-32368	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,513
essv26024892	duplication	DGMQ-31452	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,384
essv26044053	duplication	DGMQ-31226	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,486
essv25942259	duplication	DGMQ-32325	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,499
essv25912055	duplication	DGMQ-31108	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,594
essv26030643	duplication	DGMQ-31269	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,508
essv25963843	duplication	DGMQ-32977	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,525
essv26009293	duplication	DGMQ-31552	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,615
essv25977679	duplication	DGMQ-31455	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,590
essv25993629	duplication	DGMQ-31537	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,606
essv25894628	duplication	DGMQ-32145	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,532
essv25908664	duplication	DGMQ-31611	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,480
essv25979465	duplication	DGMQ-31872	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,597
essv26045737	duplication	DGMQ-31514	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,529
essv25963845	duplication	DGMQ-32977	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,525
essv26009294	duplication	DGMQ-31552	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,615
essv25894639	duplication	DGMQ-32145	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,532
essv25951602	duplication	DGMQ-32056	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,667
essv25995350	duplication	DGMQ-31529	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,515
essv26026557	duplication	DGMQ-31582	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,592
essv26030654	duplication	DGMQ-31269	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,508
essv25910360	duplication	DGMQ-32368	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,513
essv25963846	duplication	DGMQ-32977	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,525
essv25977680	duplication	DGMQ-31455	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,590
essv25979467	duplication	DGMQ-31872	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,597
essv26009295	duplication	DGMQ-31552	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,615
essv26045738	duplication	DGMQ-31514	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,529
essv26011108	duplication	DGMQ-31601	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,666
essv26044055	duplication	DGMQ-31226	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,486
essv25912056	duplication	DGMQ-31108	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,594
essv26011109	duplication	DGMQ-31601	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,666
essv25894650	duplication	DGMQ-32145	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,532
essv26044056	duplication	DGMQ-31226	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,486
essv26026558	duplication	DGMQ-31582	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,592
essv26045739	duplication	DGMQ-31514	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,529
essv26024893	duplication	DGMQ-31452	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,384
essv25995351	duplication	DGMQ-31529	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,515
essv25912057	duplication	DGMQ-31108	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,594
essv25908665	duplication	DGMQ-31611	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,480
essv25993630	duplication	DGMQ-31537	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,606
essv26042361	duplication	DGMQ-31574	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,528
essv25977681	duplication	DGMQ-31455	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,590
essv25942261	duplication	DGMQ-32325	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,499
essv25951603	duplication	DGMQ-32056	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,667
essv25910362	duplication	DGMQ-32368	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,513
essv26009296	duplication	DGMQ-31552	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,615
essv25979468	duplication	DGMQ-31872	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,597
essv26030666	duplication	DGMQ-31269	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,508
essv25963847	duplication	DGMQ-32977	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,525
essv25912058	duplication	DGMQ-31108	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,594
essv25910363	duplication	DGMQ-32368	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,513
essv25894661	duplication	DGMQ-32145	SNP array, Sequencing	Other, Probe signal intensity, Read depth	3	1,532

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Stop	Outer Stop
essv25962657	Remapped	Good	NT_187576.1:g.(418 161_?)_(527444_?)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	418,161	527,444	-
essv25951601	Remapped	Perfect	NT_187576.1:g.(429 611_?)_(?_483461)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	429,611	-	483,461
essv25995349	Remapped	Perfect	NT_187576.1:g.(429 611_?)_(?_483461)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	429,611	-	483,461
essv26011107	Remapped	Perfect	NT_187576.1:g.(429 661_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	429,661	-	483,411
essv26026554	Remapped	Perfect	NT_187576.1:g.(429 661_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	429,661	-	483,411
essv26042360	Remapped	Perfect	NT_187576.1:g.(429 661_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	429,661	-	483,411
essv26045736	Remapped	Perfect	NT_187576.1:g.(429 711_?)_(?_435561)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	429,711	-	435,561
essv25910359	Remapped	Perfect	NT_187576.1:g.(430 211_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,211	-	483,411
essv26024892	Remapped	Perfect	NT_187576.1:g.(430 311_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,311	-	483,411
essv26044053	Remapped	Perfect	NT_187576.1:g.(430 361_?)_(?_483261)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,361	-	483,261
essv25942259	Remapped	Perfect	NT_187576.1:g.(430 361_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,361	-	483,411
essv25912055	Remapped	Perfect	NT_187576.1:g.(430 561_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,561	-	483,411
essv26030643	Remapped	Perfect	NT_187576.1:g.(430 561_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,561	-	483,411
essv25963843	Remapped	Perfect	NT_187576.1:g.(430 661_?)_(?_450411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,661	-	450,411
essv26009293	Remapped	Perfect	NT_187576.1:g.(430 661_?)_(?_450461)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,661	-	450,461
essv25977679	Remapped	Perfect	NT_187576.1:g.(430 661_?)_(?_483361)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,661	-	483,361
essv25993629	Remapped	Perfect	NT_187576.1:g.(430 661_?)_(?_483361)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,661	-	483,361
essv25894628	Remapped	Perfect	NT_187576.1:g.(430 661_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,661	-	483,411
essv25908664	Remapped	Perfect	NT_187576.1:g.(430 661_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,661	-	483,411
essv25979465	Remapped	Perfect	NT_187576.1:g.(430 661_?)_(?_483461)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	430,661	-	483,461
essv26045737	Remapped	Perfect	NT_187576.1:g.(435 611_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	435,611	-	483,411
essv25963845	Remapped	Perfect	NT_187576.1:g.(451 411_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	451,411	-	483,411
essv26009294	Remapped	Perfect	NT_187576.1:g.(451 411_?)_(?_483411)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	451,411	-	483,411
essv25894639	Remapped	Perfect	NT_187576.1:g.(488 811_?)_(?_498961)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	488,811	-	498,961
essv25951602	Remapped	Perfect	NT_187576.1:g.(488 811_?)_(?_498961)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	488,811	-	498,961
essv25995350	Remapped	Perfect	NT_187576.1:g.(488 811_?)_(?_498961)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	488,811	-	498,961
essv26026557	Remapped	Perfect	NT_187576.1:g.(489 011_?)_(?_498961)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,011	-	498,961
essv26030654	Remapped	Perfect	NT_187576.1:g.(489 011_?)_(?_498961)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,011	-	498,961
essv25910360	Remapped	Perfect	NT_187576.1:g.(489 011_?)_(?_499011)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,011	-	499,011
essv25963846	Remapped	Perfect	NT_187576.1:g.(489 011_?)_(?_499011)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,011	-	499,011
essv25977680	Remapped	Perfect	NT_187576.1:g.(489 011_?)_(?_499011)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,011	-	499,011
essv25979467	Remapped	Perfect	NT_187576.1:g.(489 011_?)_(?_499011)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,011	-	499,011
essv26009295	Remapped	Perfect	NT_187576.1:g.(489 011_?)_(?_499011)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,011	-	499,011
essv26045738	Remapped	Perfect	NT_187576.1:g.(489 061_?)_(?_498961)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,061	-	498,961
essv26011108	Remapped	Perfect	NT_187576.1:g.(489 061_?)_(?_499011)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,061	-	499,011
essv26044055	Remapped	Perfect	NT_187576.1:g.(489 111_?)_(?_498961)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,111	-	498,961
essv25912056	Remapped	Perfect	NT_187576.1:g.(489 161_?)_(?_499011)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	489,161	-	499,011
essv26011109	Remapped	Perfect	NT_187576.1:g.(504 811_?)_(?_517911)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,811	-	517,911
essv25894650	Remapped	Perfect	NT_187576.1:g.(504 861_?)_(?_517911)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,861	-	517,911
essv26044056	Remapped	Perfect	NT_187576.1:g.(504 861_?)_(?_520111)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,861	-	520,111
essv26026558	Remapped	Perfect	NT_187576.1:g.(504 861_?)_(?_520211)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,861	-	520,211
essv26045739	Remapped	Perfect	NT_187576.1:g.(504 911_?)_(?_518111)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,911	-	518,111
essv26024893	Remapped	Perfect	NT_187576.1:g.(504 911_?)_(?_520061)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,911	-	520,061
essv25995351	Remapped	Perfect	NT_187576.1:g.(504 911_?)_(?_520211)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,911	-	520,211
essv25912057	Remapped	Perfect	NT_187576.1:g.(504 961_?)_(?_516961)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,961	-	516,961
essv25908665	Remapped	Perfect	NT_187576.1:g.(504 961_?)_(?_517811)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,961	-	517,811
essv25993630	Remapped	Perfect	NT_187576.1:g.(504 961_?)_(?_517911)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,961	-	517,911
essv26042361	Remapped	Perfect	NT_187576.1:g.(504 961_?)_(?_518211)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,961	-	518,211
essv25977681	Remapped	Perfect	NT_187576.1:g.(504 961_?)_(?_519511)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,961	-	519,511
essv25942261	Remapped	Perfect	NT_187576.1:g.(504 961_?)_(?_520211)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,961	-	520,211
essv25951603	Remapped	Perfect	NT_187576.1:g.(504 961_?)_(?_520211)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	504,961	-	520,211
essv25910362	Remapped	Perfect	NT_187576.1:g.(505 011_?)_(?_517811)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	505,011	-	517,811
essv26009296	Remapped	Perfect	NT_187576.1:g.(505 011_?)_(?_518061)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	505,011	-	518,061
essv25979468	Remapped	Perfect	NT_187576.1:g.(505 011_?)_(?_519561)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	505,011	-	519,561
essv26030666	Remapped	Perfect	NT_187576.1:g.(505 011_?)_(?_520111)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	505,011	-	520,111
essv25963847	Remapped	Perfect	NT_187576.1:g.(505 011_?)_(?_520211)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	505,011	-	520,211
essv25912058	Remapped	Perfect	NT_187576.1:g.(517 011_?)_(?_520211)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	517,011	-	520,211
essv25910363	Remapped	Perfect	NT_187576.1:g.(517 861_?)_(?_520211)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	517,861	-	520,211
essv25894661	Remapped	Perfect	NT_187576.1:g.(517 961_?)_(?_520261)d up	GRCh38.p12	First Pass	NT_187576.1	Chr8\|NT_18 7576.1	517,961	-	520,261
essv25962657	Submitted genomic		NC_000008.10:g.(21 82951_?)_(?_229770 0)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,182,951	-	2,297,700
essv25951601	Submitted genomic		NC_000008.10:g.(21 94401_?)_(?_224825 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,194,401	-	2,248,251
essv25995349	Submitted genomic		NC_000008.10:g.(21 94401_?)_(?_224825 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,194,401	-	2,248,251
essv26011107	Submitted genomic		NC_000008.10:g.(21 94451_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,194,451	-	2,248,201
essv26026554	Submitted genomic		NC_000008.10:g.(21 94451_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,194,451	-	2,248,201
essv26042360	Submitted genomic		NC_000008.10:g.(21 94451_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,194,451	-	2,248,201
essv26045736	Submitted genomic		NC_000008.10:g.(21 94501_?)_(?_220035 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,194,501	-	2,200,351
essv25910359	Submitted genomic		NC_000008.10:g.(21 95001_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,001	-	2,248,201
essv26024892	Submitted genomic		NC_000008.10:g.(21 95101_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,101	-	2,248,201
essv26044053	Submitted genomic		NC_000008.10:g.(21 95151_?)_(?_224805 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,151	-	2,248,051
essv25942259	Submitted genomic		NC_000008.10:g.(21 95151_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,151	-	2,248,201
essv25912055	Submitted genomic		NC_000008.10:g.(21 95351_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,351	-	2,248,201
essv26030643	Submitted genomic		NC_000008.10:g.(21 95351_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,351	-	2,248,201
essv25963843	Submitted genomic		NC_000008.10:g.(21 95451_?)_(?_221520 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,451	-	2,215,201
essv26009293	Submitted genomic		NC_000008.10:g.(21 95451_?)_(?_221525 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,451	-	2,215,251
essv25977679	Submitted genomic		NC_000008.10:g.(21 95451_?)_(?_224815 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,451	-	2,248,151
essv25993629	Submitted genomic		NC_000008.10:g.(21 95451_?)_(?_224815 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,451	-	2,248,151
essv25894628	Submitted genomic		NC_000008.10:g.(21 95451_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,451	-	2,248,201
essv25908664	Submitted genomic		NC_000008.10:g.(21 95451_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,451	-	2,248,201
essv25979465	Submitted genomic		NC_000008.10:g.(21 95451_?)_(?_224825 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,195,451	-	2,248,251
essv26045737	Submitted genomic		NC_000008.10:g.(22 00401_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,200,401	-	2,248,201
essv25963845	Submitted genomic		NC_000008.10:g.(22 16201_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,216,201	-	2,248,201
essv26009294	Submitted genomic		NC_000008.10:g.(22 16201_?)_(?_224820 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,216,201	-	2,248,201
essv25894639	Submitted genomic		NC_000008.10:g.(22 53601_?)_(?_226375 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,601	-	2,263,751
essv25951602	Submitted genomic		NC_000008.10:g.(22 53601_?)_(?_226375 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,601	-	2,263,751
essv25995350	Submitted genomic		NC_000008.10:g.(22 53601_?)_(?_226375 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,601	-	2,263,751
essv26026557	Submitted genomic		NC_000008.10:g.(22 53801_?)_(?_226375 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,801	-	2,263,751
essv26030654	Submitted genomic		NC_000008.10:g.(22 53801_?)_(?_226375 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,801	-	2,263,751
essv25910360	Submitted genomic		NC_000008.10:g.(22 53801_?)_(?_226380 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,801	-	2,263,801
essv25963846	Submitted genomic		NC_000008.10:g.(22 53801_?)_(?_226380 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,801	-	2,263,801
essv25977680	Submitted genomic		NC_000008.10:g.(22 53801_?)_(?_226380 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,801	-	2,263,801
essv25979467	Submitted genomic		NC_000008.10:g.(22 53801_?)_(?_226380 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,801	-	2,263,801
essv26009295	Submitted genomic		NC_000008.10:g.(22 53801_?)_(?_226380 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,801	-	2,263,801
essv26045738	Submitted genomic		NC_000008.10:g.(22 53851_?)_(?_226375 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,851	-	2,263,751
essv26011108	Submitted genomic		NC_000008.10:g.(22 53851_?)_(?_226380 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,851	-	2,263,801
essv26044055	Submitted genomic		NC_000008.10:g.(22 53901_?)_(?_226375 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,901	-	2,263,751
essv25912056	Submitted genomic		NC_000008.10:g.(22 53951_?)_(?_226380 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,253,951	-	2,263,801
essv26011109	Submitted genomic		NC_000008.10:g.(22 69601_?)_(?_228270 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,269,601	-	2,282,701
essv25894650	Submitted genomic		NC_000008.10:g.(22 69651_?)_(?_228270 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,269,651	-	2,282,701
essv26044056	Submitted genomic		NC_000008.10:g.(22 69651_?)_(?_228490 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,269,651	-	2,284,901
essv26026558	Submitted genomic		NC_000008.10:g.(22 69651_?)_(?_228500 1)dup	GRCh37 (hg19)		NC_000008.10	Chr8	2,269,651	-	2,285,001

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dbVar

Database of genomic structural variation

esv3975639

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant