A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704388



Internal ID128054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79442964..79455948hg38UCSC Ensembl
chr15:79735306..79748290hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3812985
hg1912985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532685
Supporting Variants
Samples
Known GenesKIAA1024
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704388
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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