A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9203



Internal ID15500429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:27157533..27164927hg38UCSC Ensembl
Outerchr15:27402680..27410074hg19UCSC Ensembl
Outerchr15:24985426..24992820hg18UCSC Ensembl
Outerchr15:24985426..24992820hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg387395
hg197395
hg187395
hg177395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23233, nssv25984, nssv22469, nssv25613, nssv20482, nssv21663, nssv21456, nssv22247, nssv22195, nssv21830, nssv25308, nssv21354, nssv21092, nssv23450, nssv22008, nssv22948, nssv22688, nssv19600, nssv22365, nssv19849, nssv27177, nssv21926, nssv19685, nssv25197, nssv20141, nssv24999, nssv24203, nssv24246, nssv21676, nssv22054
SamplesNA12802, NA18975, NA19173, NA10839, NA10847, NA18972, NA18517, NA19144, NA18860, NA07029, NA10863, NA12155, NA18563, NA12740, NA07048, NA18537, NA18572, NA18502, NA12872, NA18504, NA18564, NA18942, NA19221, NA18552, NA19132, NA11830, NA19240, NA18853, NA19007, NA18980
Known GenesGABRG3
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)nsv9203
Frequency
Sample Size31
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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