A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26460



Internal ID15844108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:30951469..30954352hg38UCSC Ensembl
Outerchr13:30941325..30954845hg38UCSC Ensembl
Innerchr13:31525606..31528489hg19UCSC Ensembl
Outerchr13:31515462..31528982hg19UCSC Ensembl
Innerchr13:30423606..30426489hg18UCSC Ensembl
Outerchr13:30413462..30426982hg18UCSC Ensembl
Innerchr13:30423606..30426489hg17UCSC Ensembl
Outerchr13:30413462..30426982hg17UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3813521
hg1913521
hg1813521
hg1713521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9063
Supporting Variants
SamplesNA19221
Known GenesTEX26
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)nssv26460
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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