A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9261



Internal ID15847173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:45073665..45074858hg38UCSC Ensembl
Outerchr15:45365863..45367056hg19UCSC Ensembl
Outerchr15:43153155..43154348hg18UCSC Ensembl
Outerchr15:43153155..43154348hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381194
hg191194
hg181194
hg171194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26017, nssv26207, nssv27492, nssv25744
SamplesNA18502, NA18860, NA19221, NA19132
Known GenesSORD
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)nsv9261
Frequency
Sample Size31
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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