A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9156



Internal ID15500382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:77671798..77674371hg38UCSC Ensembl
Outerchr14:78138141..78140714hg19UCSC Ensembl
Outerchr14:77207894..77210467hg18UCSC Ensembl
Outerchr14:77207894..77210467hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382574
hg192574
hg182574
hg172574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21558
SamplesNA18564
Known GenesALKBH1
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)nsv9156
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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