A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598878



Internal ID21790923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64371888..64371888hg38UCSC Ensembl
chr15:64664087..64664087hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090730
Supporting Variants
Samples
Known GenesKIAA0101
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598878
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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