A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2893479



Internal ID15421448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763277..155773949hg38UCSC Ensembl
Innerchr3:155481066..155491738hg19UCSC Ensembl
Innerchr3:156963760..156974432hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3810673
hg1910673
hg1810673
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514997
Supporting Variants
SamplesNA19225
Known GenesC3orf33
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2893479
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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