nsv6625120

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:50
Validation:Not tested
Clinical Assertions: No
Region Size:29,788

Publication(s):Zarrei et al. 2023

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: 989 SVs from 80 studies. See in: genome view

Remapped(Score: Perfect):40,850,341-40,880,128

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6625120	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nsv6625120	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	41,356,246	41,386,033

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18281922	deletion	OSC2271	SNP array	Probe signal intensity	nssv18281923, nssv18281925, nssv18281924
nssv18282011	deletion	OSC2088	SNP array	Probe signal intensity	6
nssv18282018	deletion	OSC2096	SNP array	Probe signal intensity	7
nssv18282841	deletion	OSC2254	SNP array	Probe signal intensity	8
nssv18283215	deletion	OSC2308	SNP array	Probe signal intensity	8
nssv18283795	deletion	OSC2278	SNP array	Probe signal intensity	nssv18283794
nssv18283953	deletion	OSC2382	SNP array	Probe signal intensity	6
nssv18285465	deletion	OSC2781	SNP array	Probe signal intensity	nssv18286373, nssv18286374
nssv18285607	deletion	OSC2881	SNP array	Probe signal intensity	nssv18286187
nssv18285765	deletion	OSC2849	SNP array	Probe signal intensity	14
nssv18286442	deletion	OSC2826	SNP array	Probe signal intensity	5
nssv18287603	deletion	OSC3009	SNP array	Probe signal intensity	nssv18287604, nssv18287602, nssv18286702
nssv18288049	deletion	OSC3288	SNP array	Probe signal intensity	6
nssv18288128	deletion	OSC3185	SNP array	Probe signal intensity	11
nssv18289325	deletion	OSC3381	SNP array	Probe signal intensity	nssv18289326
nssv18289478	deletion	OSC3484	SNP array	Probe signal intensity	8
nssv18289583	deletion	OSC3568	SNP array	Probe signal intensity	9
nssv18289601	deletion	OSC0371	SNP array	Probe signal intensity	nssv18289600, nssv18291172
nssv18290330	deletion	OSC3608	SNP array	Probe signal intensity	nssv18291214, nssv18290568, nssv18290331
nssv18290356	deletion	OSC3624	SNP array	Probe signal intensity	nssv18291238, nssv18291237
nssv18290518	deletion	OSC3747	SNP array	Probe signal intensity	6
nssv18290598	deletion	OSC3625	SNP array	Probe signal intensity	7
nssv18290714	deletion	OSC3704	SNP array	Probe signal intensity	9
nssv18290945	deletion	OSC3630	SNP array	Probe signal intensity	7
nssv18292272	deletion	OSC0403	SNP array	Probe signal intensity	nssv18291916, nssv18291683, nssv18291923
nssv18292577	deletion	OSC3918	SNP array	Probe signal intensity	6
nssv18293191	deletion	OSC0430	SNP array	Probe signal intensity	7
nssv18293917	deletion	OSC0433	SNP array	Probe signal intensity	8
nssv18295579	deletion	OSC4551	SNP array	Probe signal intensity	6
nssv18296081	deletion	OSC0484	SNP array	Probe signal intensity	8
nssv18300156	deletion	OSC0551	SNP array	Probe signal intensity	nssv18299470
nssv18300400	deletion	OSC0577	SNP array	Probe signal intensity	7
nssv18302564	deletion	OSC0600	SNP array	Probe signal intensity	6
nssv18304452	deletion	OSC0635	SNP array	Probe signal intensity	12
nssv18310841	deletion	OSC0769	SNP array	Probe signal intensity	9
nssv18312032	deletion	OSC0788	SNP array	Probe signal intensity	6
nssv18319948	deletion	OSC0972	SNP array	Probe signal intensity	5
nssv18320278	deletion	OSC0951	SNP array	Probe signal intensity	6
nssv18320611	deletion	OSC0098	SNP array	Probe signal intensity	9
nssv18322628	deletion	OSC1319	SNP array	Probe signal intensity	nssv18322894
nssv18322679	deletion	OSC1350	SNP array	Probe signal intensity	7
nssv18324012	deletion	OSC1654	SNP array	Probe signal intensity	9
nssv18324066	deletion	OSC1689	SNP array	Probe signal intensity	9
nssv18324392	deletion	OSC1719	SNP array	Probe signal intensity	nssv18324110, nssv18324393
nssv18324421	deletion	OSC1740	SNP array	Probe signal intensity	6
nssv18324589	deletion	OSC1659	SNP array	Probe signal intensity	7
nssv18324662	deletion	OSC1705	SNP array	Probe signal intensity	9
nssv18324927	deletion	OSC1895	SNP array	Probe signal intensity	nssv18325576, nssv18325836, nssv18325837
nssv18324947	deletion	OSC1910	SNP array	Probe signal intensity	nssv18324948, nssv18324946, nssv18325854
nssv18326013	deletion	OSC2014	SNP array	Probe signal intensity	nssv18326015, nssv18326014, nssv18326269

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18281922	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18282011	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18282018	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18282841	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18283215	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18283795	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18283953	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18285465	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18285607	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18285765	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18286442	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18287603	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18288049	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18288128	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18289325	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18289478	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18289583	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18289601	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18290330	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18290356	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18290518	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18290598	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18290714	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18290945	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18292272	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18292577	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18293191	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18293917	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18295579	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18296081	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18300156	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18300400	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18302564	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18304452	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18310841	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18312032	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18319948	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18320278	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18320611	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18322628	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18322679	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18324012	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18324066	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18324392	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18324421	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18324589	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18324662	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18324927	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18324947	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18326013	Remapped	Perfect	NC_000019.10:g.(?_ 40850341)_(4088012 8_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,850,341	40,880,128
nssv18281922	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18282011	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18282018	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18282841	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18283215	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18283795	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18283953	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18285465	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18285607	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18285765	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18286442	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18287603	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18288049	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18288128	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18289325	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18289478	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18289583	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18289601	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18290330	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18290356	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18290518	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18290598	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18290714	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18290945	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18292272	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18292577	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18293191	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18293917	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18295579	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18296081	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18300156	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18300400	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18302564	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18304452	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18310841	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18312032	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18319948	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18320278	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18320611	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18322628	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18322679	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18324012	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18324066	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18324392	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18324421	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18324589	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18324662	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18324927	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18324947	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033
nssv18326013	Submitted genomic		NC_000019.9:g.(?_4 1356246)_(41386033 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	41,356,246	41,386,033

dbVar

Database of genomic structural variation

nsv6625120

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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