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dbVar

Database of genomic structural variation

nsv5922139

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:65

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: 101 SVs from 20 studies. See in: genome view

Submitted genomic111,603,641-111,603,705

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5922139	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	111,603,641	111,603,705
nsv5922139	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	111,474,365	111,474,429

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17355287	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17355287	Submitted genomic		NC_000011.10:g.111 603641_111603705de l	GRCh38 (hg38)		NC_000011.10	Chr11	111,603,641	111,603,705
nssv17355287	Remapped	Perfect	NC_000011.9:g.1114 74365_111474429del	GRCh37.p13	First Pass	NC_000011.9	Chr11	111,474,365	111,474,429

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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