A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023593



Internal ID83444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34029451..34030561hg38UCSC Ensembl
chr9:34029449..34030559hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381111
hg191111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475837
Supporting Variants
Samples
Known GenesUBAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023593
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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