A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2807412



Internal ID15341073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73543359..73545863hg38UCSC Ensembl
Innerchr14:74010063..74012567hg19UCSC Ensembl
Innerchr14:73079816..73082320hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382505
hg192505
hg182505
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514749
Supporting Variants
SamplesNA18622
Known GenesACOT1, HEATR4
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2807412
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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