A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26349



Internal ID15491372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84150575..84516232hg38UCSC Ensembl
Outerchr15:84146793..84527916hg38UCSC Ensembl
Innerchr15:84819327..85059463hg19UCSC Ensembl
Outerchr15:84815545..85071147hg19UCSC Ensembl
Innerchr15:82610331..82860467hg18UCSC Ensembl
Outerchr15:82606549..82872151hg18UCSC Ensembl
Innerchr15:82610331..82860467hg17UCSC Ensembl
Outerchr15:82606549..82872151hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38381124
hg19255603
hg18265603
hg17265603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9290
Supporting Variants
SamplesNA18860
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC100505679, LOC388152, LOC440300, LOC642423, 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)nssv26349
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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