A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18628



Internal ID15842476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67014712..67031921hg38UCSC Ensembl
Outerchr9:67011524..67034189hg38UCSC Ensembl
Innerchr9:40660920..40678129hg19UCSC Ensembl
Outerchr9:40658652..40681317hg19UCSC Ensembl
Innerchr9:40650920..40668129hg18UCSC Ensembl
Outerchr9:40648652..40671317hg18UCSC Ensembl
Innerchr9:40390203..40407412hg17UCSC Ensembl
Outerchr9:40387935..40410600hg17UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3822666
hg1922666
hg1822666
hg1722666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8456
Supporting Variants
SamplesNA19144
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)nssv18628
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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