A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26207



Internal ID15837945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45074094..45074188hg38UCSC Ensembl
Outerchr15:45073665..45074858hg38UCSC Ensembl
Innerchr15:45366292..45366386hg19UCSC Ensembl
Outerchr15:45365863..45367056hg19UCSC Ensembl
Innerchr15:43153584..43153678hg18UCSC Ensembl
Outerchr15:43153155..43154348hg18UCSC Ensembl
Innerchr15:43153584..43153678hg17UCSC 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 StatusS
Merged Variantsnsv9261
Supporting Variants
SamplesNA18860
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)nssv26207
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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