A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18728



Internal ID15830880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67140832..67216417hg38UCSC Ensembl
Outerchr9:67140318..67216978hg38UCSC Ensembl
Innerchr9:40476424..40552009hg19UCSC Ensembl
Outerchr9:40475863..40552523hg19UCSC Ensembl
Innerchr9:40466424..40542009hg18UCSC Ensembl
Outerchr9:40465863..40542523hg18UCSC Ensembl
Innerchr9:40205707..40281292hg17UCSC Ensembl
Outerchr9:40205146..40281806hg17UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3876661
hg1976661
hg1876661
hg1776661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8456
Supporting Variants
SamplesNA12155
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)nssv18728
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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