A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602583



Internal ID21794630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25686249..25687233hg38UCSC Ensembl
chr15:25931396..25932380hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026160
Supporting Variants
Samples
Known GenesATP10A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602583
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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