A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2818444



Internal ID15744195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20345387..20432547hg38UCSC Ensembl
Innerchr15:20550640..20637800hg19UCSC Ensembl
Innerchr15:18810654..18897814hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3887161
hg1987161
hg1887161
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514762
Supporting Variants
SamplesNA19147
Known GenesHERC2P3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2818444
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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