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dbVar

Database of genomic structural variation

nsv5912769

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:84

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

Submitted genomic95,863,298-95,863,381

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5912769	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	95,863,298	95,863,381
nsv5912769	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	95,492,610	95,492,693

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17447483	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17447483	Submitted genomic		NC_000007.14:g.958 63298_95863381del	GRCh38 (hg38)		NC_000007.14	Chr7	95,863,298	95,863,381
nssv17447483	Remapped	Perfect	NC_000007.13:g.954 92610_95492693del	GRCh37.p13	First Pass	NC_000007.13	Chr7	95,492,610	95,492,693

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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