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dbVar

Database of genomic structural variation

nsv5896870

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:129

Publication(s):Almarri et al. 2020

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: 123 SVs from 27 studies. See in: genome view

Submitted genomic171,618,719-171,618,847

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5896870	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	171,618,719	171,618,847
nsv5896870	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	171,336,509	171,336,637

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17412046	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17412046	Submitted genomic		NC_000003.12:g.171 618719_171618847de l	GRCh38 (hg38)		NC_000003.12	Chr3	171,618,719	171,618,847
nssv17412046	Remapped	Perfect	NC_000003.11:g.171 336509_171336637de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	171,336,509	171,336,637

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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