A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2806061



Internal ID15635196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73556527..73557503hg38UCSC Ensembl
Innerchr14:74023231..74024207hg19UCSC Ensembl
Innerchr14:73092984..73093960hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38977
hg19977
hg18977
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514750
Supporting Variants
SamplesNA12376
Known GenesHEATR4
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2806061
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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