A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462



Internal ID15827209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81905510..81906229hg38UCSC Ensembl
Outerchr9:81904795..81911698hg38UCSC Ensembl
Innerchr9:84520425..84521144hg19UCSC Ensembl
Outerchr9:84519710..84526613hg19UCSC Ensembl
Innerchr9:83710245..83710964hg18UCSC Ensembl
Outerchr9:83709530..83716433hg18UCSC Ensembl
Innerchr9:81749979..81750698hg17UCSC Ensembl
Outerchr9:81749264..81756167hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg386904
hg196904
hg186904
hg176904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8534
Supporting Variants
SamplesNA07029
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)nssv17462
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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