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dbVar

Database of genomic structural variation

nsv5925799

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:312

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: 143 SVs from 29 studies. See in: genome view

Submitted genomic76,314,861-76,315,172

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5925799	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	76,314,861	76,315,172
nsv5925799	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	78,929,777	78,930,088

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17446000	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17446000	Submitted genomic		NC_000009.12:g.763 14861_76315172del	GRCh38 (hg38)		NC_000009.12	Chr9	76,314,861	76,315,172
nssv17446000	Remapped	Perfect	NC_000009.11:g.789 29777_78930088del	GRCh37.p13	First Pass	NC_000009.11	Chr9	78,929,777	78,930,088

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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