A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9259



Internal ID15847171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:45025170..45034152hg38UCSC Ensembl
Outerchr15:45317368..45326350hg19UCSC Ensembl
Outerchr15:43104660..43113642hg18UCSC Ensembl
Outerchr15:43104660..43113642hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388983
hg198983
hg188983
hg178983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv26158, nssv27484, nssv23618, nssv22307, nssv22854, nssv22006, nssv24726, nssv20602, nssv24441, nssv22496, nssv22605, nssv22188, nssv25354, nssv25692, nssv25347
SamplesNA18504, NA18563, NA18860, NA18942, NA19007, NA19221, NA18537, NA19132, NA18517, NA18564, NA19240, NA19144, NA19173, NA18972, NA18552
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)nsv9259
Frequency
Sample Size31
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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