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dbVar

Database of genomic structural variation

nsv5925924

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:73

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: 135 SVs from 26 studies. See in: genome view

Submitted genomic59,002,184-59,002,256

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5925924	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	59,002,184	59,002,256
nsv5925924	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	59,914,743	59,914,815

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17433089	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17433089	Submitted genomic		NC_000008.11:g.590 02184_59002256del	GRCh38 (hg38)		NC_000008.11	Chr8	59,002,184	59,002,256
nssv17433089	Remapped	Perfect	NC_000008.10:g.599 14743_59914815del	GRCh37.p13	First Pass	NC_000008.10	Chr8	59,914,743	59,914,815

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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