Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6631160

Organism: Homo sapiens

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

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:97,903

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: 1359 SVs from 103 studies. See in: genome view

Remapped(Score: Perfect):31,392,478-31,490,380

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6631160	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	31,392,478	31,490,380
nsv6631160	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	31,360,255	31,458,157

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18296943	duplication	OSC0501	SNP array	Probe signal intensity	8
nssv18322006	deletion	OSC1147	SNP array	Probe signal intensity	10

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18296943	Remapped	Perfect	NC_000006.12:g.(?_ 31392478)_(3149038 0_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	31,392,478	31,490,380
nssv18322006	Remapped	Perfect	NC_000006.12:g.(?_ 31392478)_(3149038 0_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	31,392,478	31,490,380
nssv18296943	Submitted genomic		NC_000006.11:g.(?_ 31360255)_(3145815 7_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	31,360,255	31,458,157
nssv18322006	Submitted genomic		NC_000006.11:g.(?_ 31360255)_(3145815 7_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	31,360,255	31,458,157

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

You are here: NCBI