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dbVar

Database of genomic structural variation

nsv5920269

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:59

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

Submitted genomic42,979,546-42,979,604

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5920269	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	42,979,546	42,979,604
nsv5920269	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	42,834,689	42,834,747

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17440350	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17440350	Submitted genomic		NC_000008.11:g.429 79546_42979604del	GRCh38 (hg38)		NC_000008.11	Chr8	42,979,546	42,979,604
nssv17440350	Remapped	Perfect	NC_000008.10:g.428 34689_42834747del	GRCh37.p13	First Pass	NC_000008.10	Chr8	42,834,689	42,834,747

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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