A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9153



Internal ID15500379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:73525409..73587026hg38UCSC Ensembl
Outerchr14:73992113..74053730hg19UCSC Ensembl
Outerchr14:73061866..73123483hg18UCSC Ensembl
Outerchr14:73061866..73123483hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3861618
hg1961618
hg1861618
hg1761618
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24762, nssv22037, nssv20976, nssv21286, nssv22328, nssv21634, nssv19535, nssv21528, nssv26766, nssv21226, nssv20946, nssv21350, nssv24769, nssv24744, nssv22049, nssv24940, nssv21685, nssv22007, nssv19000, nssv20372, nssv21715, nssv22035, nssv24794, nssv21498, nssv20432, nssv19942, nssv22297, nssv24089, nssv19565, nssv19030, nssv22209, nssv24773, nssv23798, nssv25278, nssv20874, nssv19882, nssv21256, nssv21243, nssv22065, nssv19661, nssv21236, nssv19912, nssv23825, nssv19489, nssv22998, nssv24748, nssv19972, nssv20904, nssv24062
SamplesNA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, NA12740, NA19173, NA18972, NA18552
Known GenesACOT1, ACOT2, HEATR4
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)nsv9153
Frequency
Sample Size31
Observed Gain29
Observed Loss13
Observed Complex0
Frequencyn/a


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