nsv4371117

Organism: Homo sapiens

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

Variant Calls:49
Validation:Not tested
Clinical Assertions: No
Region Size:100,770

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: 1042 SVs from 101 studies. See in: genome view

Remapped(Score: Perfect):38,254,487-38,355,256

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4371117	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nsv4371117	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	38,294,088	38,394,857

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15612038	copy number gain	1-0642-003	SNP array	Genotyping	19
nssv15613663	copy number gain	1-0121-003	SNP array	Genotyping	31
nssv15613827	copy number gain	1-0707-002	SNP array	Genotyping	22
nssv15627315	copy number gain	1-0057-002	SNP array	Genotyping	20
nssv15627761	copy number gain	1-0004-004	SNP array	Genotyping	20
nssv15634448	copy number gain	11-0041-003	SNP array	Genotyping	19
nssv15635146	copy number gain	13-0029-002	SNP array	Genotyping	18
nssv15642192	copy number gain	16-1002-001	SNP array	Genotyping	20
nssv15643805	copy number gain	15-1134-004	SNP array	Genotyping	29
nssv15644612	copy number gain	15-1134-002	SNP array	Genotyping	25
nssv15644665	copy number gain	16-1000-002	SNP array	Genotyping	25
nssv15645852	copy number gain	2-0273-004	SNP array	Genotyping	20
nssv15645943	copy number gain	2-0295-003	SNP array	Genotyping	21
nssv15649455	copy number gain	2-1401-003	SNP array	Genotyping	30
nssv15655407	copy number gain	3-0107-000	SNP array	Genotyping	21
nssv15655475	copy number gain	3-0178-000	SNP array	Genotyping	25
nssv15663038	copy number gain	4-0043-003	SNP array	Genotyping	23
nssv15668653	copy number gain	7-0212-003	SNP array	Genotyping	19
nssv15671831	copy number gain	9-0017-003	SNP array	Genotyping	13
nssv15673927	copy number gain	9-0025-002	SNP array	Genotyping	22
nssv15675077	copy number gain	217292	SNP array	Genotyping	27
nssv15675599	copy number gain	170789	SNP array	Genotyping	21
nssv15675844	copy number gain	209352	SNP array	Genotyping	33
nssv15677456	copy number gain	163536	SNP array	Genotyping	25
nssv15678873	copy number gain	176004	SNP array	Genotyping	29
nssv15680493	copy number gain	193290	SNP array	Genotyping	25
nssv15680546	copy number gain	214097	SNP array	Genotyping	19
nssv15680683	copy number gain	215270	SNP array	Genotyping	21
nssv15681011	copy number gain	181218	SNP array	Genotyping	19
nssv15682039	copy number gain	216161	SNP array	Genotyping	22
nssv15682325	copy number gain	OCD11-S_896192	SNP array	Genotyping	17
nssv15683888	copy number gain	OCD136-896482	SNP array	Genotyping	16
nssv15683905	copy number gain	OCD136-896483	SNP array	Genotyping	15
nssv15686876	copy number gain	OCD35-S_0555-6300-2	SNP array	Genotyping	18
nssv15686952	copy number gain	OCD37-S_0625-0201-3	SNP array	Genotyping	21
nssv15688262	copy number gain	210241	SNP array	Genotyping	23
nssv15688482	copy number gain	OCD32-S_896583	SNP array	Genotyping	38
nssv15688715	copy number gain	OCD44-B_AH-1374	SNP array	Genotyping	19
nssv15690985	copy number gain	OCD18-S_896353	SNP array	Genotyping	21
nssv15691029	copy number gain	OCD23-S_896432	SNP array	Genotyping	17
nssv15691048	copy number gain	OCD23-S_896433	SNP array	Genotyping	19
nssv15691132	copy number gain	OCD26-896511	SNP array	Genotyping	28
nssv15693138	copy number gain	OCD85-896842	SNP array	Genotyping	21
nssv15693852	copy number gain	OCD70-896292	SNP array	Genotyping	28
nssv15697044	copy number gain	127821	SNP array	Genotyping	26
nssv15697253	copy number gain	160093	SNP array	Genotyping	19
nssv15698877	copy number gain	182591	SNP array	Genotyping	15
nssv15701143	copy number gain	183323	SNP array	Genotyping	26
nssv15702454	copy number gain	169112	SNP array	Genotyping	24

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15612038	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15613663	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15613827	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15627315	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15627761	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15634448	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15635146	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15642192	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15643805	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15644612	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15644665	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15645852	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15645943	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15649455	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15655407	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15655475	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15663038	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15668653	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15671831	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15673927	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15675077	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15675599	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15675844	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15677456	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15678873	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15680493	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15680546	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15680683	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15681011	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15682039	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15682325	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15683888	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15683905	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15686876	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15686952	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15688262	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15688482	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15688715	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15690985	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15691029	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15691048	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15691132	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15693138	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15693852	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15697044	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15697253	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15698877	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15701143	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15702454	Remapped	Perfect	NC_000007.14:g.(?_ 38254487)_(3835525 6_?)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	38,254,487	38,355,256
nssv15612038	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15613663	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15613827	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15627315	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15627761	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15634448	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15635146	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15642192	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15643805	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15644612	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15644665	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15645852	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15645943	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15649455	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15655407	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15655475	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15663038	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15668653	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15671831	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15673927	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15675077	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15675599	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15675844	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15677456	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15678873	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15680493	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15680546	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15680683	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15681011	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15682039	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15682325	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15683888	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15683905	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15686876	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15686952	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15688262	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15688482	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15688715	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15690985	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15691029	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15691048	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15691132	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15693138	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15693852	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15697044	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15697253	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15698877	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15701143	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857
nssv15702454	Submitted genomic		NC_000007.13:g.(?_ 38294088)_(3839485 7_?)dup	GRCh37 (hg19)		NC_000007.13	Chr7	38,294,088	38,394,857

dbVar

Database of genomic structural variation

nsv4371117

Links to Other Resources

Genome View

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