A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732155



Internal ID155821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35213927..35213978hg38UCSC Ensembl
chr20:33801730..33801781hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551742
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732155
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012176


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