A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23852



Internal ID15833791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74105399..74121975hg38UCSC Ensembl
Outerchr14:74102835..74131200hg38UCSC Ensembl
Innerchr14:74572102..74588678hg19UCSC Ensembl
Outerchr14:74569538..74597903hg19UCSC Ensembl
Innerchr14:73641855..73658431hg18UCSC Ensembl
Outerchr14:73639291..73667656hg18UCSC Ensembl
Innerchr14:73641855..73658431hg17UCSC Ensembl
Outerchr14:73639291..73667656hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3828366
hg1928366
hg1828366
hg1728366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9154
Supporting Variants
SamplesNA18504
Known GenesLIN52
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv23852
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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