A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25142



Internal ID15834429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24862254..24863687hg38UCSC Ensembl
Outerchr15:24861811..24873253hg38UCSC Ensembl
Innerchr15:25107401..25108834hg19UCSC Ensembl
Outerchr15:25106958..25118400hg19UCSC Ensembl
Innerchr15:22658494..22659927hg18UCSC Ensembl
Outerchr15:22658051..22669493hg18UCSC Ensembl
Innerchr15:22658494..22659927hg17UCSC Ensembl
Outerchr15:22658051..22669493hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3811443
hg1911443
hg1811443
hg1711443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9199
Supporting Variants
SamplesNA18517
Known GenesSNRPN
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)nssv25142
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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