A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911430



Internal ID8386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36701038..36701089hg38UCSC Ensembl
chr2:36928181..36928232hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5406322
Supporting Variants
Samples
Known GenesVIT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911430
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.018576


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