A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20652



Internal ID15833132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137303489..137320912hg38UCSC Ensembl
Outerchr9:137303248..137322124hg38UCSC Ensembl
Innerchr9:140197941..140215364hg19UCSC Ensembl
Outerchr9:140197700..140216576hg19UCSC Ensembl
Innerchr9:139317762..139335185hg18UCSC Ensembl
Outerchr9:139317521..139336397hg18UCSC Ensembl
Innerchr9:137473778..137491201hg17UCSC Ensembl
Outerchr9:137473537..137492413hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3818877
hg1918877
hg1818877
hg1718877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8583
Supporting Variants
SamplesNA18502
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)nssv20652
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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