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dbVar

Database of genomic structural variation

nsv5926257

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:1,377

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: 181 SVs from 40 studies. See in: genome view

Submitted genomic114,605,043-114,606,419

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5926257	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	114,605,043	114,606,419
nsv5926257	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	114,475,765	114,477,141

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17361809	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17361809	Submitted genomic		NC_000011.10:g.114 605043_114606419de l	GRCh38 (hg38)		NC_000011.10	Chr11	114,605,043	114,606,419
nssv17361809	Remapped	Perfect	NC_000011.9:g.1144 75765_114477141del	GRCh37.p13	First Pass	NC_000011.9	Chr11	114,475,765	114,477,141

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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