A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600081



Internal ID21792128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25847466..25847466hg38UCSC Ensembl
chr15:26092613..26092613hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090025
Supporting Variants
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600081
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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