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dbVar

Database of genomic structural variation

nsv4636776

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:6,001

Description:nsv4248653 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: 95 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):14,023,683-14,029,683

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4636776	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	14,023,683	14,029,683
nsv4636776	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	13,927,000	13,933,000

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16164881	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16164881	Remapped	Perfect	NC_000017.11:g.140 23683_14029683del	GRCh38.p12	First Pass	NC_000017.11	Chr17	14,023,683	14,029,683
nssv16164881	Submitted genomic		NC_000017.10:g.139 27000_13933000del	GRCh37 (hg19)		NC_000017.10	Chr17	13,927,000	13,933,000

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)
nssv16164881	0.014	262	18876

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