nsv4379443

Organism: Homo sapiens

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

Variant Calls:53
Validation:Not tested
Clinical Assertions: No
Region Size:37,472

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: 1964 SVs from 105 studies. See in: genome view

Remapped(Score: Perfect):29,869,381-29,906,852

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4379443	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nsv4379443	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	29,837,158	29,874,629

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15613076	copy number loss	1-0663-003	SNP array	Genotyping	8
nssv15616065	copy number gain	1-0781-003	SNP array	Genotyping	18
nssv15626944	copy number loss	1-0458-001	SNP array	Genotyping	20
nssv15627334	copy number loss	1-0057-003	SNP array	Genotyping	21
nssv15630082	copy number loss	1-0632-003	SNP array	Genotyping	19
nssv15631612	copy number loss	10-0001-001	SNP array	Genotyping	24
nssv15632133	copy number loss	10-0011-002	SNP array	Genotyping	28
nssv15632376	copy number loss	10-0004-001	SNP array	Genotyping	13
nssv15632993	copy number loss	10-1090-001	SNP array	Genotyping	26
nssv15634554	copy number gain	12-4261-003	SNP array	Genotyping	28
nssv15635205	copy number gain	13-0031-004	SNP array	Genotyping	19
nssv15635920	copy number gain	12-4261-001	SNP array	Genotyping	20
nssv15640424	copy number gain	14-0286-002	SNP array	Genotyping	20
nssv15641951	copy number gain	15-1126-003	SNP array	Genotyping	18
nssv15642127	copy number gain	16-1001-001	SNP array	Genotyping	28
nssv15642992	copy number gain	15-1131-002	SNP array	Genotyping	21
nssv15643957	copy number gain	16-1009-001	SNP array	Genotyping	30
nssv15648269	copy number loss	2-1244-001	SNP array	Genotyping	24
nssv15653024	copy number gain	2-1583-003	SNP array	Genotyping	27
nssv15667121	copy number gain	7-0119-003	SNP array	Genotyping	13
nssv15668484	copy number gain	7-0223-003	SNP array	Genotyping	23
nssv15669216	copy number gain	7-0140-003	SNP array	Genotyping	24
nssv15669998	copy number gain	7-0280-006	SNP array	Genotyping	22
nssv15674757	copy number gain	205648	SNP array	Genotyping	18
nssv15675048	copy number loss	209351	SNP array	Genotyping	35
nssv15675362	copy number gain	232822S	SNP array	Genotyping	20
nssv15679612	copy number loss	182123	SNP array	Genotyping	24
nssv15682363	copy number loss	OCD110-B_1654	SNP array	Genotyping	23
nssv15682387	copy number loss	OCD110-S_1652	SNP array	Genotyping	26
nssv15682674	copy number loss	OCD1127-715	SNP array	Genotyping	18
nssv15682807	copy number loss	OCD1154-S_HAM513	SNP array	Genotyping	18
nssv15683609	copy number loss	OCD130-8961053	SNP array	Genotyping	23
nssv15683639	copy number loss	OCD131-8961082	SNP array	Genotyping	16
nssv15683654	copy number loss	OCD137-0625-2972-2	SNP array	Genotyping	28
nssv15683982	copy number loss	OCD138-0625-3695-2	SNP array	Genotyping	21
nssv15684249	copy number loss	OCD112-S_1666	SNP array	Genotyping	13
nssv15686930	copy number loss	OCD37-S_0625-0201-2	SNP array	Genotyping	24
nssv15687208	copy number loss	OCD39-S_0625-1152-2	SNP array	Genotyping	27
nssv15687676	copy number loss	OCD172-SW-1812	SNP array	Genotyping	17
nssv15690222	copy number loss	OCD132-8961111	SNP array	Genotyping	26
nssv15690255	copy number loss	OCD132-8961113	SNP array	Genotyping	18
nssv15690459	copy number loss	OCD143-MH-1300(189271)	SNP array	Genotyping	18
nssv15692946	copy number loss	OCD79-896722	SNP array	Genotyping	14
nssv15693135	copy number loss	OCD85-896842	SNP array	Genotyping	21
nssv15693504	copy number loss	OCD71-896302	SNP array	Genotyping	22
nssv15693952	copy number loss	OCD97-1400-2	SNP array	Genotyping	19
nssv15694079	copy number loss	214314	SNP array	Genotyping	21
nssv15694283	copy number loss	OCD84-896822	SNP array	Genotyping	23
nssv15694556	copy number loss	79220	SNP array	Genotyping	14
nssv15694815	copy number loss	199160	SNP array	Genotyping	20
nssv15699525	copy number gain	155498	SNP array	Genotyping	20
nssv15702390	copy number loss	153923	SNP array	Genotyping	22
nssv15702895	copy number loss	202163	SNP array	Genotyping	29

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15613076	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15616065	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15626944	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15627334	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15630082	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15631612	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15632133	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15632376	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15632993	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15634554	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15635205	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15635920	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15640424	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15641951	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15642127	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15642992	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15643957	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15648269	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15653024	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15667121	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15668484	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15669216	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15669998	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15674757	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15675048	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15675362	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15679612	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15682363	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15682387	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15682674	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15682807	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15683609	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15683639	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15683654	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15683982	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15684249	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15686930	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15687208	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15687676	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15690222	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15690255	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15690459	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15692946	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15693135	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15693504	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15693952	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15694079	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15694283	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15694556	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15694815	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15699525	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15702390	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15702895	Remapped	Perfect	NC_000006.12:g.(?_ 29869381)_(2990685 2_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,869,381	29,906,852
nssv15613076	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15616065	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15626944	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15627334	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15630082	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15631612	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15632133	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15632376	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15632993	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15634554	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15635205	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15635920	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15640424	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15641951	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15642127	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15642992	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15643957	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15648269	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15653024	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15667121	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15668484	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15669216	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15669998	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15674757	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15675048	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15675362	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15679612	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15682363	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15682387	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15682674	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15682807	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15683609	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15683639	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15683654	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15683982	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15684249	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15686930	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15687208	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15687676	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15690222	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15690255	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15690459	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15692946	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15693135	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15693504	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15693952	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629
nssv15694079	Submitted genomic		NC_000006.11:g.(?_ 29837158)_(2987462 9_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,837,158	29,874,629

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dbVar

Database of genomic structural variation

nsv4379443

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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