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dbVar

Database of genomic structural variation

nsv4637736

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:108,201

Description:nsv4187398 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: 679 SVs from 77 studies. See in: genome view

Remapped(Score: Perfect):61,518,962-61,627,162

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4637736	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	61,518,962	61,627,162
nsv4637736	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	44,726,800	44,835,000

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16167494	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16167494	Remapped	Perfect	NC_000009.12:g.615 18962_61627162del	GRCh38.p12	First Pass	NC_000009.12	Chr9	61,518,962	61,627,162
nssv16167494	Submitted genomic		NC_000009.11:g.447 26800_44835000del	GRCh37 (hg19)		NC_000009.11	Chr9	44,726,800	44,835,000

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)
nssv16167494	0.093	2022	21694

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