A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910208



Internal ID7579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20904475..20931372hg38UCSC Ensembl
chr2:21104235..21131132hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3826898
hg1926898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910208
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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