A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043078



Internal ID96427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32624717..32627513hg38UCSC Ensembl
chr11:32646263..32649059hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382797
hg192797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494401
Supporting Variants
Samples
Known GenesCCDC73
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043078
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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