A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26076



Internal ID15485998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84527916..84531609hg38UCSC Ensembl
Outerchr15:84516232..84533618hg38UCSC Ensembl
Innerchr15:85071147..85074840hg19UCSC Ensembl
Outerchr15:85059463..85076849hg19UCSC Ensembl
Innerchr15:82872151..82875844hg18UCSC Ensembl
Outerchr15:82860467..82877853hg18UCSC Ensembl
Innerchr15:82872151..82875844hg17UCSC Ensembl
Outerchr15:82860467..82877853hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3817387
hg1917387
hg1817387
hg1717387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9290
Supporting Variants
SamplesNA18502
Known GenesGOLGA6L5P, UBE2Q2P1
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)nssv26076
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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