A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9181



Internal ID15847093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:23174492..23226025hg38UCSC Ensembl
Outerchr15:22647043..22701513hg19UCSC Ensembl
Outerchr15:20198407..20252877hg18UCSC Ensembl
Outerchr15:20198407..20252877hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3851534
hg1954471
hg1854471
hg1754471
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21276, nssv22229, nssv19300, nssv19991, nssv22289, nssv22245, nssv20792, nssv27057, nssv25345, nssv25053, nssv21590, nssv21620, nssv21934, nssv22539, nssv24098, nssv22259, nssv25688, nssv22567
SamplesNA18502, NA11830, NA07029, NA18504, NA12802, NA18860, NA10839, NA10863, NA12872, NA19221, NA18537, NA18853, NA19132, NA12740, NA19173
Known GenesMIR4509-1, MIR4509-2, MIR4509-3
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)nsv9181
Frequency
Sample Size31
Observed Gain8
Observed Loss8
Observed Complex0
Frequencyn/a


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