A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9063



Internal ID15846975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:30941325..30954845hg38UCSC Ensembl
Outerchr13:31515462..31528982hg19UCSC Ensembl
Outerchr13:30413462..30426982hg18UCSC 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 StatusM
Merged Variants
Supporting Variantsnssv26460
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)nsv9063
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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