A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911179



Internal ID8220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21599231..21635209hg38UCSC Ensembl
chr2:21822103..21858081hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3835979
hg1935979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435988
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911179
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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