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dbVar

Database of genomic structural variation

nsv6301087

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:81,694

Description:nsv6140481 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: 1207 SVs from 78 studies. See in: genome view

Remapped(Score: Perfect):162,145,043-162,226,736

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6301087	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	162,145,043	162,226,736
nsv6301087	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	162,566,075	162,647,768

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17651536	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17651536	Remapped	Perfect	NC_000006.12:g.162 145043_162226736de l	GRCh38.p12	First Pass	NC_000006.12	Chr6	162,145,043	162,226,736
nssv17651536	Submitted genomic		NC_000006.11:g.162 566075_162647768de l	GRCh37 (hg19)		NC_000006.11	Chr6	162,566,075	162,647,768

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)
nssv17651536	0.016	101	6404

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