A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26158



Internal ID15838674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45025716..45032573hg38UCSC Ensembl
Outerchr15:45025170..45032991hg38UCSC Ensembl
Innerchr15:45317914..45324771hg19UCSC Ensembl
Outerchr15:45317368..45325189hg19UCSC Ensembl
Innerchr15:43105206..43112063hg18UCSC Ensembl
Outerchr15:43104660..43112481hg18UCSC Ensembl
Innerchr15:43105206..43112063hg17UCSC Ensembl
Outerchr15:43104660..43112481hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg387822
hg197822
hg187822
hg177822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9259
Supporting Variants
SamplesNA18860
Known GenesSORD
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)nssv26158
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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