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dbVar

Database of genomic structural variation

nsv5961371

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:296

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: 121 SVs from 21 studies. See in: genome view

Submitted genomic45,876,095-45,876,390

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961371	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	45,876,095	45,876,390
nsv5961371	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	44,504,734	44,505,029

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17394074	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17394074	Submitted genomic		NC_000020.11:g.458 76095_45876390del	GRCh38 (hg38)		NC_000020.11	Chr20	45,876,095	45,876,390
nssv17394074	Remapped	Perfect	NC_000020.10:g.445 04734_44505029del	GRCh37.p13	First Pass	NC_000020.10	Chr20	44,504,734	44,505,029

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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