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dbVar

Database of genomic structural variation

nsv6112833

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:17,705

Description:nsv5432539 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: 295 SVs from 60 studies. See in: genome view

Remapped(Score: Perfect):72,060,682-72,078,386

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112833	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	72,060,682	72,078,386
nsv6112833	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	72,094,581	72,112,285

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17965064	copy number variation	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17965064	Remapped	Perfect	GRCh38.p12	First Pass	NC_000016.10	Chr16	72,060,682	72,078,386
nssv17965064	Submitted genomic		GRCh37 (hg19)		NC_000016.9	Chr16	72,094,581	72,112,285

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)
nssv17965064	0.051	87	1692

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