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dbVar

Database of genomic structural variation

nsv5915241

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:325

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: 463 SVs from 42 studies. See in: genome view

Submitted genomic137,257,814-137,258,138

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5915241	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	137,257,814	137,258,138
nsv5915241	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	140,152,266	140,152,590

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17449013	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17449013	Submitted genomic		NC_000009.12:g.137 257814_137258138de l	GRCh38 (hg38)		NC_000009.12	Chr9	137,257,814	137,258,138
nssv17449013	Remapped	Perfect	NC_000009.11:g.140 152266_140152590de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	140,152,266	140,152,590

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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