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dbVar

Database of genomic structural variation

nsv5897068

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:66

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: 183 SVs from 40 studies. See in: genome view

Submitted genomic80,902,423-80,902,488

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5897068	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	80,902,423	80,902,488
nsv5897068	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	81,823,577	81,823,642

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17428236	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17428236	Submitted genomic		NC_000004.12:g.809 02423_80902488del	GRCh38 (hg38)		NC_000004.12	Chr4	80,902,423	80,902,488
nssv17428236	Remapped	Perfect	NC_000004.11:g.818 23577_81823642del	GRCh37.p13	First Pass	NC_000004.11	Chr4	81,823,577	81,823,642

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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