A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9193



Internal ID15847105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:23809267..23995586hg38UCSC Ensembl
Outerchr15:24054414..24240733hg19UCSC Ensembl
Outerchr15:21605507..21791826hg18UCSC Ensembl
Outerchr15:21605507..21791826hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38186320
hg19186320
hg18186320
hg17186320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23121, nssv25258, nssv21336, nssv21324, nssv22599, nssv19360, nssv21948, nssv27117, nssv24220, nssv19625, nssv21994, nssv24151, nssv22379, nssv22217, nssv21686, nssv24974, nssv20332, nssv20111, nssv20972, nssv25806, nssv22305, nssv25067, nssv19789, nssv22015, nssv21646, nssv21800, nssv21633, nssv23364, nssv22890
SamplesNA11830, 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 Genes
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)nsv9193
Frequency
Sample Size31
Observed Gain29
Observed Loss0
Observed Complex0
Frequencyn/a


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