A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046



Internal ID15835290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61996971..62149738hg38UCSC Ensembl
Outerchr9:61996785..62149738hg38UCSC Ensembl
Innerchr9:65957607..66149353hg17UCSC Ensembl
Outerchr9:65957144..66149539hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38152954
hg17192396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8499
Supporting Variants
SamplesNA18552
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)nssv18046
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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