A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20382



Internal ID15832884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40298061..40328676hg38UCSC Ensembl
Outerchr9:40293928..40329508hg38UCSC Ensembl
Innerchr9:43028207..43058824hg19UCSC Ensembl
Outerchr9:43027375..43062956hg19UCSC Ensembl
Innerchr9:43018203..43048820hg18UCSC Ensembl
Outerchr9:43017371..43052952hg18UCSC Ensembl
Innerchr9:45593357..45623972hg17UCSC Ensembl
Outerchr9:45589224..45624804hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3835581
hg1935582
hg1835582
hg1735581
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8486
Supporting Variants
SamplesNA18502
Known GenesFAM95B1
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)nssv20382
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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