A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9250



Internal ID15847162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43600811..43604249hg38UCSC Ensembl
Outerchr15:43893009..43896447hg19UCSC Ensembl
Outerchr15:41680301..41683739hg18UCSC Ensembl
Outerchr15:41680301..41683739hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg383439
hg193439
hg183439
hg173439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24562
SamplesNA19240
Known GenesRNU6-28P, 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)nsv9250
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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