A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732113



Internal ID155779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34621043..34621395hg38UCSC Ensembl
chr20:33208847..33209199hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561820
Supporting Variants
Samples
Known GenesPIGU
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732113
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.010459


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