A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037514



Internal ID92764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72222916..72223598hg38UCSC Ensembl
chr10:73982674..73983356hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480903
Supporting Variants
Samples
Known GenesANAPC16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037514
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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