A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022737



Internal ID82846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76831142..76837984hg38UCSC Ensembl
chr9:79446058..79452900hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg386843
hg196843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481422
Supporting Variants
Samples
Known GenesPRUNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022737
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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