A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9676



Internal ID15500902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:20613896..20619995hg38UCSC Ensembl
Outerchr19:20796702..20802801hg19UCSC Ensembl
Outerchr19:20588542..20594641hg18UCSC Ensembl
Outerchr19:20588542..20594641hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg386100
hg196100
hg186100
hg176100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24841, nssv25672
SamplesNA19173, NA18564
Known GenesZNF626
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)nsv9676
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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