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dbVar

Database of genomic structural variation

nsv5893524

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:4,753

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: 121 SVs from 25 studies. See in: genome view

Submitted genomic30,756,138-30,760,890

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5893524	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	30,756,138	30,760,890
nsv5893524	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	30,757,760	30,762,512

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17416407	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17416407	Submitted genomic		NC_000004.12:g.307 56138_30760890del	GRCh38 (hg38)		NC_000004.12	Chr4	30,756,138	30,760,890
nssv17416407	Remapped	Perfect	NC_000004.11:g.307 57760_30762512del	GRCh37.p13	First Pass	NC_000004.11	Chr4	30,757,760	30,762,512

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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