A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732131



Internal ID155797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34889400..34889502hg38UCSC Ensembl
chr20:33477203..33477305hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528533
Supporting Variants
Samples
Known GenesACSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732131
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.489697


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