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dbVar

Database of genomic structural variation

nsv4642578

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:79

Description:nsv4243563 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: 89 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):21,027,257-21,027,335

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4642578	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	21,027,257	21,027,335
nsv4642578	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	20,930,570	20,930,648

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16177746	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16177746	Remapped	Perfect	NC_000017.11:g.210 27257_21027335del	GRCh38.p12	First Pass	NC_000017.11	Chr17	21,027,257	21,027,335
nssv16177746	Submitted genomic		NC_000017.10:g.209 30570_20930648del	GRCh37 (hg19)		NC_000017.10	Chr17	20,930,570	20,930,648

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)
nssv16177746	0.014	312	21688

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