A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19782



Internal ID15832769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38859978..38874436hg38UCSC Ensembl
Outerchr9:38859777..38874542hg38UCSC Ensembl
Innerchr9:38859975..38874433hg19UCSC Ensembl
Outerchr9:38859774..38874539hg19UCSC Ensembl
Innerchr9:38849975..38864433hg18UCSC Ensembl
Outerchr9:38849774..38864539hg18UCSC Ensembl
Innerchr9:38849975..38864433hg17UCSC Ensembl
Outerchr9:38849774..38864539hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3814766
hg1914766
hg1814766
hg1714766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8446
Supporting Variants
SamplesNA18502
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)nssv19782
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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