A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20442



Internal ID15832933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62123260..62147005hg38UCSC Ensembl
Outerchr9:62122969..62148766hg38UCSC Ensembl
Innerchr9:65999296..66023060hg17UCSC Ensembl
Outerchr9:65997534..66023351hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3825798
hg1725818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8499
Supporting Variants
SamplesNA18502
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)nssv20442
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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