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dbVar

Database of genomic structural variation

nsv6120788

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:267

Description:nsv5497623 from Byrska-Bishop et. al 2021. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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: 169 SVs from 42 studies. See in: genome view

Remapped(Score: Perfect):131,032,719-131,032,985

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6120788	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	131,032,719	131,032,985
nsv6120788	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	131,517,264	131,517,530

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17962549	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17962549	Remapped	Perfect	NC_000012.12:g.131 032719_131032985de l	GRCh38.p12	First Pass	NC_000012.12	Chr12	131,032,719	131,032,985
nssv17962549	Submitted genomic		NC_000012.11:g.131 517264_131517530de l	GRCh37 (hg19)		NC_000012.11	Chr12	131,517,264	131,517,530

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17962549	0.059	376	6404

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