A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731981



Internal ID155647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32761048..32761320hg38UCSC Ensembl
chr20:31348854..31349126hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731981
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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