A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097050



Internal ID21277971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77168639..77176870hg38UCSC Ensembl
Innerchr15:77460981..77469212hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg388232
hg198232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116839
Supporting Variants
Samplessample262
Known GenesPEAK1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097050
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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