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dbVar

Database of genomic structural variation

nsv6297481

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:1,543

Description:nsv5440068 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: 160 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):182,577,168-182,578,710

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6297481	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	182,577,168	182,578,710
nsv6297481	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	182,546,303	182,547,845

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17655035	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17655035	Remapped	Perfect	NC_000001.11:g.182 577168_182578710de l	GRCh38.p12	First Pass	NC_000001.11	Chr1	182,577,168	182,578,710
nssv17655035	Submitted genomic		NC_000001.10:g.182 546303_182547845de l	GRCh37 (hg19)		NC_000001.10	Chr1	182,546,303	182,547,845

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)
nssv17655035	0.089	571	6404

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