A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731907



Internal ID155573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31500710..31576566hg38UCSC Ensembl
chr20:30088513..30164369hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3875857
hg1975857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528607
Supporting Variants
Samples
Known GenesHM13, HM13-AS1, PSIMCT-1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731907
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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