A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22066



Internal ID15488914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82353915..82359303hg38UCSC Ensembl
Outerchr15:82353412..82359429hg38UCSC Ensembl
Innerchr15:82646136..82651522hg19UCSC Ensembl
Outerchr15:82645642..82651648hg19UCSC Ensembl
Innerchr15:80433191..80438577hg18UCSC Ensembl
Outerchr15:80432697..80438703hg18UCSC Ensembl
Innerchr15:80433191..80438577hg17UCSC Ensembl
Outerchr15:80432697..80438703hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386018
hg196007
hg186007
hg176007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9284
Supporting Variants
SamplesNA18552
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)nssv22066
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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