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dbVar

Database of genomic structural variation

nsv6302267

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:12,285

Description:nsv5457540 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: 685 SVs from 54 studies. See in: genome view

Remapped(Score: Perfect):162,194,354-162,206,638

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6302267	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	162,194,354	162,206,638
nsv6302267	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	162,615,386	162,627,670

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17676560	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17676560	Remapped	Perfect	NC_000006.12:g.162 194354_162206638de l	GRCh38.p12	First Pass	NC_000006.12	Chr6	162,194,354	162,206,638
nssv17676560	Submitted genomic		NC_000006.11:g.162 615386_162627670de l	GRCh37 (hg19)		NC_000006.11	Chr6	162,615,386	162,627,670

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)
nssv17676560	0.894	5729	6404

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