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dbVar

Database of genomic structural variation

nsv5890782

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:103

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: 95 SVs from 24 studies. See in: genome view

Submitted genomic41,170,658-41,170,760

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5890782	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	41,170,658	41,170,760
nsv5890782	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	41,172,675	41,172,777

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17426322	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17426322	Submitted genomic		NC_000004.12:g.411 70658_41170760del	GRCh38 (hg38)		NC_000004.12	Chr4	41,170,658	41,170,760
nssv17426322	Remapped	Perfect	NC_000004.11:g.411 72675_41172777del	GRCh37.p13	First Pass	NC_000004.11	Chr4	41,172,675	41,172,777

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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