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dbVar

Database of genomic structural variation

nsv6297100

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:127,375

Description:nsv5423972 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: 493 SVs from 64 studies. See in: genome view

Remapped(Score: Perfect):155,047,651-155,175,025

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6297100	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	155,047,651	155,175,025
nsv6297100	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	155,020,127	155,147,501

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17676958	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17676958	Remapped	Perfect	NC_000001.11:g.155 047651_155175025du p	GRCh38.p12	First Pass	NC_000001.11	Chr1	155,047,651	155,175,025
nssv17676958	Submitted genomic		NC_000001.10:g.155 020127_155147501du p	GRCh37 (hg19)		NC_000001.10	Chr1	155,020,127	155,147,501

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)
nssv17676958	0.015	95	6400

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