A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21903



Internal ID15481525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82358403..82361689hg38UCSC Ensembl
Outerchr15:82357216..82362497hg38UCSC Ensembl
Innerchr15:82650581..82653917hg19UCSC Ensembl
Outerchr15:82649432..82654728hg19UCSC Ensembl
Innerchr15:80437636..80440972hg18UCSC Ensembl
Outerchr15:80436487..80441783hg18UCSC Ensembl
Innerchr15:80437636..80440972hg17UCSC Ensembl
Outerchr15:80436487..80441783hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg385282
hg195297
hg185297
hg175297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9284
Supporting Variants
SamplesNA07048
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)nssv21903
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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