A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9273



Internal ID15500499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68370605..68372944hg38UCSC Ensembl
Outerchr15:68662943..68665282hg19UCSC Ensembl
Outerchr15:66449997..66452336hg18UCSC Ensembl
Outerchr15:66449997..66452336hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382340
hg192340
hg182340
hg172340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22190, nssv25788, nssv20261
SamplesNA12872, NA19132, NA18853
Known GenesITGA11
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)nsv9273
Frequency
Sample Size31
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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