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dbVar

Database of genomic structural variation

nsv4634440

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:69,233

Description:nsv4143086 from gnomAD Structural Variants. 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: 2557 SVs from 97 studies. See in: genome view

Remapped(Score: Perfect):78,257,470-78,326,702

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4634440	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	78,257,470	78,326,702
nsv4634440	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	78,967,187	79,036,419

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16164756	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16164756	Remapped	Perfect	NC_000006.12:g.782 57470_78326702del	GRCh38.p12	First Pass	NC_000006.12	Chr6	78,257,470	78,326,702
nssv16164756	Submitted genomic		NC_000006.11:g.789 67187_79036419del	GRCh37 (hg19)		NC_000006.11	Chr6	78,967,187	79,036,419

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)
nssv16164756	0.16	3465	21694

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