A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26298



Internal ID15491337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82352734..82388639hg38UCSC Ensembl
Outerchr15:82351990..82396777hg38UCSC Ensembl
Innerchr15:82644963..82680852hg19UCSC Ensembl
Outerchr15:82644219..82688988hg19UCSC Ensembl
Innerchr15:80432018..80467907hg18UCSC Ensembl
Outerchr15:80431274..80476043hg18UCSC Ensembl
Innerchr15:80432018..80467907hg17UCSC Ensembl
Outerchr15:80431274..80476043hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3844788
hg1944770
hg1844770
hg1744770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9284
Supporting Variants
SamplesNA18860
Known GenesUBE2Q2P2, UBE2Q2P3
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)nssv26298
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer