A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255



Internal ID15834603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40483114..40487666hg38UCSC Ensembl
Outerchr9:40482829..40488837hg38UCSC Ensembl
Innerchr9:42869260..42873810hg19UCSC Ensembl
Outerchr9:42868090..42874095hg19UCSC Ensembl
Innerchr9:42859256..42863806hg18UCSC Ensembl
Outerchr9:42858086..42864091hg18UCSC Ensembl
Innerchr9:45778380..45782930hg17UCSC Ensembl
Outerchr9:45778095..45784100hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386009
hg196006
hg186006
hg176006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8488
Supporting Variants
SamplesNA18537
Known GenesAQP7P3
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)nssv18255
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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