A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607583



Internal ID21799630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79438110..79438216hg38UCSC Ensembl
chr15:79730452..79730558hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026929
Supporting Variants
Samples
Known GenesKIAA1024
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607583
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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