A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2806130



Internal ID15613515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73535999..73536359hg38UCSC Ensembl
Innerchr14:74002703..74003063hg19UCSC Ensembl
Innerchr14:73072456..73072816hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38361
hg19361
hg18361
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514747
Supporting Variants
SamplesNA11894
Known GenesHEATR4
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2806130
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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