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dbVar

Database of genomic structural variation

nsv5925623

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:98

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: 122 SVs from 32 studies. See in: genome view

Submitted genomic122,867,212-122,867,309

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5925623	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	122,867,212	122,867,309
nsv5925623	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	125,629,491	125,629,588

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17430246	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17430246	Submitted genomic		NC_000009.12:g.122 867212_122867309de l	GRCh38 (hg38)		NC_000009.12	Chr9	122,867,212	122,867,309
nssv17430246	Remapped	Perfect	NC_000009.11:g.125 629491_125629588de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	125,629,491	125,629,588

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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