A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734880



Internal ID158546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81505421..81512290hg38UCSC Ensembl
chr3:81554572..81561441hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg386870
hg196870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452067
Supporting Variants
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734880
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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