A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19805



Internal ID15482236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34455884..34499018hg38UCSC Ensembl
Outerchr15:34455172..34499459hg38UCSC Ensembl
Innerchr15:34748085..34791219hg19UCSC Ensembl
Outerchr15:34747373..34791660hg19UCSC Ensembl
Innerchr15:32535377..32578511hg18UCSC Ensembl
Outerchr15:32534665..32578952hg18UCSC Ensembl
Innerchr15:32535377..32578511hg17UCSC Ensembl
Outerchr15:32534665..32578952hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3844288
hg1944288
hg1844288
hg1744288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA10847
Known Genes
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)nssv19805
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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