A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9251



Internal ID15500477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43618769..43660722hg38UCSC Ensembl
Outerchr15:43910967..43952920hg19UCSC Ensembl
Outerchr15:41698259..41740212hg18UCSC Ensembl
Outerchr15:41698259..41740212hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3841954
hg1941954
hg1841954
hg1741954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24648
SamplesNA19240
Known GenesCATSPER2, STRC
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)nsv9251
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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