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dbVar

Database of genomic structural variation

nsv5991440

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:64

Publication(s):Wu et al. 2021

Links to Other Resources

Overlapping Genes

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 26 studies. See in: genome view

Submitted genomic112,005,873-112,005,936

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5991440	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	112,005,873	112,005,936
nsv5991440	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	111,724,720	111,724,783

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17549623	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17549623	Submitted genomic		NC_000003.12:g.112 005873_112005936de l	GRCh38 (hg38)		NC_000003.12	Chr3	112,005,873	112,005,936
nssv17549623	Remapped	Perfect	NC_000003.11:g.111 724720_111724783de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	111,724,720	111,724,783

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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