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dbVar

Database of genomic structural variation

nsv5391568

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:1,921

Description:nsv4850745 from Abel et. al 2020. 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: 113 SVs from 37 studies. See in: genome view

Remapped(Score: Perfect):23,643,253-23,645,173

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5391568	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	23,643,253	23,645,173
nsv5391568	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	23,654,574	23,656,494

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16883946	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16883946	Remapped	Perfect	NC_000016.10:g.236 43253_23645173del	GRCh38.p12	First Pass	NC_000016.10	Chr16	23,643,253	23,645,173
nssv16883946	Submitted genomic		NC_000016.9:g.2365 4574_23656494del	GRCh37 (hg19)		NC_000016.9	Chr16	23,654,574	23,656,494

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)
nssv16883946	0.011	183	16834

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