A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116084



Internal ID21299350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:80057965..80068824hg38UCSC Ensembl
Innerchr15:80350307..80361166hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3810860
hg1910860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098138
Samplessample392
Known GenesZFAND6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116084
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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