A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18785



Internal ID15828820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:8162796..8218511hg38UCSC Ensembl
Outerchr12:8157482..8219735hg38UCSC Ensembl
Innerchr12:8315392..8371107hg19UCSC Ensembl
Outerchr12:8310078..8372331hg19UCSC Ensembl
Innerchr12:8206659..8262374hg18UCSC Ensembl
Outerchr12:8201345..8263598hg18UCSC Ensembl
Innerchr12:8206659..8262374hg17UCSC Ensembl
Outerchr12:8201345..8263598hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3862254
hg1962254
hg1862254
hg1762254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8899
Supporting Variants
SamplesNA10847
Known GenesFAM66C, ZNF705A
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)nssv18785
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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