A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704132



Internal ID127798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89629240..89629349hg38UCSC Ensembl
chr15:90172471..90172580hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523328
Supporting Variants
Samples
Known GenesKIF7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704132
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003285


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