A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8736



Internal ID15846648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125822789..125825778hg38UCSC Ensembl
Outerchr10:127511358..127514347hg19UCSC Ensembl
Outerchr10:127501348..127504337hg18UCSC Ensembl
Outerchr10:127501348..127504337hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382990
hg192990
hg182990
hg172990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21493
SamplesNA18504
Known GenesBCCIP, UROS
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)nsv8736
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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