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dbVar

Database of genomic structural variation

nsv5921766

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:110

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: 92 SVs from 27 studies. See in: genome view

Submitted genomic47,715,819-47,715,928

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5921766	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	47,715,819	47,715,928
nsv5921766	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	47,737,371	47,737,480

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17364071	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17364071	Submitted genomic		NC_000011.10:g.477 15819_47715928del	GRCh38 (hg38)		NC_000011.10	Chr11	47,715,819	47,715,928
nssv17364071	Remapped	Perfect	NC_000011.9:g.4773 7371_47737480del	GRCh37.p13	First Pass	NC_000011.9	Chr11	47,737,371	47,737,480

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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