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dbVar

Database of genomic structural variation

nsv5888778

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:700

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: 406 SVs from 59 studies. See in: genome view

Submitted genomic196,334,822-196,335,521

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5888778	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	196,334,822	196,335,521
nsv5888778	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	196,061,693	196,062,392

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17421197	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17421197	Submitted genomic		NC_000003.12:g.196 334822_196335521de l	GRCh38 (hg38)		NC_000003.12	Chr3	196,334,822	196,335,521
nssv17421197	Remapped	Perfect	NC_000003.11:g.196 061693_196062392de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	196,061,693	196,062,392

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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