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dbVar

Database of genomic structural variation

nsv5908734

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:91

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: 136 SVs from 34 studies. See in: genome view

Submitted genomic90,891,118-90,891,208

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5908734	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	90,891,118	90,891,208
nsv5908734	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	93,653,400	93,653,490

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17441967	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17441967	Submitted genomic		NC_000009.12:g.908 91118_90891208del	GRCh38 (hg38)		NC_000009.12	Chr9	90,891,118	90,891,208
nssv17441967	Remapped	Perfect	NC_000009.11:g.936 53400_93653490del	GRCh37.p13	First Pass	NC_000009.11	Chr9	93,653,400	93,653,490

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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