nsv4366719

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:66
Validation:Not tested
Clinical Assertions: No
Region Size:25,216

Publication(s):Zarrei et al. 2019

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: 322 SVs from 64 studies. See in: genome view

Remapped(Score: Perfect):107,130,169-107,155,384

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4366719	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nsv4366719	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	108,051,326	108,076,541

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15611716	copy number loss	1-0653-003	SNP array	Genotyping	17
nssv15614334	copy number loss	1-0743-003	SNP array	Genotyping	23
nssv15616665	copy number loss	1-0864-004	SNP array	Genotyping	18
nssv15618639	copy number loss	1-0871-003	SNP array	Genotyping	16
nssv15619172	copy number loss	1-0930-003	SNP array	Genotyping	14
nssv15619188	copy number loss	1-0930-004	SNP array	Genotyping	17
nssv15622181	copy number loss	1-1060-003	SNP array	Genotyping	26
nssv15623626	copy number loss	1-0271-001	SNP array	Genotyping	24
nssv15624423	copy number loss	1-0286-004	SNP array	Genotyping	23
nssv15625044	copy number loss	1-0345-001	SNP array	Genotyping	27
nssv15628121	copy number loss	1-0534-006	SNP array	Genotyping	19
nssv15628263	copy number loss	1-0489-001	SNP array	Genotyping	21
nssv15630916	copy number loss	1-0629-003	SNP array	Genotyping	15
nssv15631700	copy number loss	10-0013-003	SNP array	Genotyping	26
nssv15634768	copy number loss	12-8115-004	SNP array	Genotyping	20
nssv15635162	copy number loss	13-0031-002	SNP array	Genotyping	22
nssv15636321	copy number loss	14-0039-003	SNP array	Genotyping	23
nssv15636342	copy number loss	14-0039-004	SNP array	Genotyping	24
nssv15637136	copy number loss	12-4855-001	SNP array	Genotyping	22
nssv15639248	copy number loss	14-0284-002	SNP array	Genotyping	25
nssv15640207	copy number loss	14-0119-004	SNP array	Genotyping	18
nssv15642333	copy number loss	14-0385-002	SNP array	Genotyping	21
nssv15643525	copy number loss	16-1013-002	SNP array	Genotyping	27
nssv15644829	copy number loss	16-1010-001	SNP array	Genotyping	24
nssv15649141	copy number loss	2-1258-001	SNP array	Genotyping	27
nssv15649481	copy number loss	2-1402-001	SNP array	Genotyping	26
nssv15650832	copy number loss	2-1402-003	SNP array	Genotyping	17
nssv15650873	copy number loss	2-1408-002	SNP array	Genotyping	22
nssv15651640	copy number loss	2-1528-001	SNP array	Genotyping	22
nssv15651684	copy number loss	2-1528-003	SNP array	Genotyping	16
nssv15651706	copy number loss	2-1546-003	SNP array	Genotyping	25
nssv15652790	copy number loss	2-1540-003	SNP array	Genotyping	28
nssv15654076	copy number loss	2-1690-002	SNP array	Genotyping	24
nssv15654988	copy number loss	2-1633-001	SNP array	Genotyping	18
nssv15655008	copy number loss	2-1633-002	SNP array	Genotyping	21
nssv15655025	copy number loss	2-1633-003	SNP array	Genotyping	15
nssv15655039	copy number loss	2-1646-003	SNP array	Genotyping	26
nssv15655140	copy number loss	2-1690-003	SNP array	Genotyping	24
nssv15655847	copy number loss	2-1743-003	SNP array	Genotyping	24
nssv15656749	copy number loss	3-0577-000	SNP array	Genotyping	18
nssv15657414	copy number loss	3-0530-000	SNP array	Genotyping	15
nssv15657599	copy number loss	4-0039-001	SNP array	Genotyping	25
nssv15658642	copy number loss	3-0542-000	SNP array	Genotyping	16
nssv15658789	copy number loss	3-0609-000	SNP array	Genotyping	13
nssv15659574	copy number loss	3-0774-000	SNP array	Genotyping	23
nssv15662754	copy number loss	5-0135-003	SNP array	Genotyping	24
nssv15665686	copy number loss	7-0084-003	SNP array	Genotyping	18
nssv15665816	copy number loss	7-0097-003	SNP array	Genotyping	19
nssv15667771	copy number loss	7-0072-003	SNP array	Genotyping	24
nssv15671386	copy number loss	7-0282-003	SNP array	Genotyping	20
nssv15671849	copy number loss	9-0018-001	SNP array	Genotyping	20
nssv15674876	copy number loss	208026	SNP array	Genotyping	20
nssv15676263	copy number loss	168475	SNP array	Genotyping	22
nssv15677747	copy number loss	234354	SNP array	Genotyping	24
nssv15679607	copy number loss	182123	SNP array	Genotyping	24
nssv15680088	copy number loss	208030	SNP array	Genotyping	21
nssv15688886	copy number loss	222691	SNP array	Genotyping	27
nssv15690508	copy number loss	OCD145-HM-1349(188527)	SNP array	Genotyping	20
nssv15690775	copy number loss	OCD160-0625-4932-2	SNP array	Genotyping	23
nssv15696526	copy number loss	159785	SNP array	Genotyping	19
nssv15698080	copy number loss	125087	SNP array	Genotyping	19
nssv15698558	copy number loss	222720	SNP array	Genotyping	24
nssv15699344	copy number loss	78729	SNP array	Genotyping	20
nssv15700501	copy number loss	181146	SNP array	Genotyping	24
nssv15700517	copy number loss	176068	SNP array	Genotyping	12
nssv15701509	copy number loss	79350	SNP array	Genotyping	23

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15611716	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15614334	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15616665	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15618639	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15619172	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15619188	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15622181	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15623626	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15624423	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15625044	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15628121	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15628263	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15630916	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15631700	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15634768	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15635162	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15636321	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15636342	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15637136	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15639248	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15640207	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15642333	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15643525	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15644829	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15649141	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15649481	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15650832	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15650873	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15651640	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15651684	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15651706	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15652790	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15654076	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15654988	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15655008	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15655025	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15655039	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15655140	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15655847	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15656749	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15657414	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15657599	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15658642	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15658789	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15659574	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15662754	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15665686	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15665816	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15667771	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15671386	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15671849	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15674876	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15676263	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15677747	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15679607	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15680088	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15688886	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15690508	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15690775	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15696526	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15698080	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15698558	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15699344	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15700501	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15700517	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15701509	Remapped	Perfect	NC_000004.12:g.(?_ 107130169)_(107155 384_?)del	GRCh38.p12	First Pass	NC_000004.12	Chr4	107,130,169	107,155,384
nssv15611716	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15614334	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15616665	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15618639	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15619172	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15619188	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15622181	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15623626	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15624423	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15625044	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15628121	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15628263	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15630916	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15631700	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15634768	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15635162	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15636321	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15636342	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15637136	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15639248	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15640207	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15642333	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15643525	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15644829	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15649141	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15649481	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15650832	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15650873	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15651640	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15651684	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15651706	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15652790	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15654076	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541
nssv15654988	Submitted genomic		NC_000004.11:g.(?_ 108051326)_(108076 541_?)del	GRCh37 (hg19)		NC_000004.11	Chr4	108,051,326	108,076,541

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dbVar

Database of genomic structural variation

nsv4366719

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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