A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731539



Internal ID155205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21478539..21478588hg38UCSC Ensembl
chr20:21459177..21459226hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731539
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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