A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22140



Internal ID15844016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67064402..67136595hg38UCSC Ensembl
Outerchr9:67063992..67137000hg38UCSC Ensembl
Innerchr9:40556246..40628439hg19UCSC Ensembl
Outerchr9:40555841..40628849hg19UCSC Ensembl
Innerchr9:40546246..40618439hg18UCSC Ensembl
Outerchr9:40545841..40618849hg18UCSC Ensembl
Innerchr9:40285529..40357722hg17UCSC Ensembl
Outerchr9:40285124..40358132hg17UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3873009
hg1973009
hg1873009
hg1773009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8456
Supporting Variants
SamplesNA19221
Known Genes
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)nssv22140
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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