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dbVar

Database of genomic structural variation

nsv5914051

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:136

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: 97 SVs from 24 studies. See in: genome view

Submitted genomic15,566,768-15,566,903

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5914051	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	15,566,768	15,566,903
nsv5914051	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	15,608,767	15,608,902

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17367357	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17367357	Submitted genomic		NC_000010.11:g.155 66768_15566903del	GRCh38 (hg38)		NC_000010.11	Chr10	15,566,768	15,566,903
nssv17367357	Remapped	Perfect	NC_000010.10:g.156 08767_15608902del	GRCh37.p13	First Pass	NC_000010.10	Chr10	15,608,767	15,608,902

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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