A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23226



Internal ID15844310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137303489..137320347hg38UCSC Ensembl
Outerchr9:137303248..137320912hg38UCSC Ensembl
Innerchr9:140197941..140214799hg19UCSC Ensembl
Outerchr9:140197700..140215364hg19UCSC Ensembl
Innerchr9:139317762..139334620hg18UCSC Ensembl
Outerchr9:139317521..139335185hg18UCSC Ensembl
Innerchr9:137473778..137490636hg17UCSC Ensembl
Outerchr9:137473537..137491201hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3817665
hg1917665
hg1817665
hg1717665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8583
Supporting Variants
SamplesNA19221
Known GenesEXD3
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)nssv23226
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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