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dbVar

Database of genomic structural variation

nsv5921870

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:323

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: 168 SVs from 47 studies. See in: genome view

Submitted genomic51,825,401-51,825,723

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5921870	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	51,825,401	51,825,723
nsv5921870	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	52,737,961	52,738,283

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17433753	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17433753	Submitted genomic		NC_000008.11:g.518 25401_51825723del	GRCh38 (hg38)		NC_000008.11	Chr8	51,825,401	51,825,723
nssv17433753	Remapped	Perfect	NC_000008.10:g.527 37961_52738283del	GRCh37.p13	First Pass	NC_000008.10	Chr8	52,737,961	52,738,283

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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