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dbVar

Database of genomic structural variation

nsv5913209

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:148

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: 162 SVs from 47 studies. See in: genome view

Submitted genomic90,841,972-90,842,119

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5913209	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	90,841,972	90,842,119
nsv5913209	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	93,604,254	93,604,401

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17439889	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17439889	Submitted genomic		NC_000009.12:g.908 41972_90842119del	GRCh38 (hg38)		NC_000009.12	Chr9	90,841,972	90,842,119
nssv17439889	Remapped	Perfect	NC_000009.11:g.936 04254_93604401del	GRCh37.p13	First Pass	NC_000009.11	Chr9	93,604,254	93,604,401

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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