A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8533



Internal ID15846445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81708348..81712130hg38UCSC Ensembl
Outerchr9:84323263..84327045hg19UCSC Ensembl
Outerchr9:83513083..83516865hg18UCSC Ensembl
Outerchr9:81552817..81556599hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg383783
hg193783
hg183783
hg173783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19978, nssv18546, nssv17576
SamplesNA19007, NA10863, NA19144
Known GenesLOC101927502
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)nsv8533
Frequency
Sample Size31
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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