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dbVar

Database of genomic structural variation

nsv5385881

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:128

Description:nsv4832275 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: 135 SVs from 36 studies. See in: genome view

Remapped(Score: Perfect):132,173,939-132,174,066

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5385881	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	132,173,939	132,174,066
nsv5385881	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	135,049,326	135,049,453

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16880360	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16880360	Remapped	Perfect	NC_000009.12:g.132 173939_132174066du p	GRCh38.p12	First Pass	NC_000009.12	Chr9	132,173,939	132,174,066
nssv16880360	Submitted genomic		NC_000009.11:g.135 049326_135049453du p	GRCh37 (hg19)		NC_000009.11	Chr9	135,049,326	135,049,453

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)
nssv16880360	0.059	993	16834

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