A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23149



Internal ID15830994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24101997..24133143hg38UCSC Ensembl
Outerchr15:24101777..24136081hg38UCSC Ensembl
Innerchr15:24347144..24378290hg19UCSC Ensembl
Outerchr15:24346924..24381228hg19UCSC Ensembl
Innerchr15:21898237..21929383hg18UCSC Ensembl
Outerchr15:21898017..21932321hg18UCSC Ensembl
Innerchr15:21898237..21929383hg17UCSC Ensembl
Outerchr15:21898017..21932321hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3834305
hg1934305
hg1834305
hg1734305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA12155
Known Genes
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)nssv23149
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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