A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20762



Internal ID15827611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22172054..22174467hg38UCSC Ensembl
Outerchr15:22171291..22174724hg38UCSC Ensembl
Innerchr15:22460005..22462418hg19UCSC Ensembl
Outerchr15:22459242..22462675hg19UCSC Ensembl
Innerchr15:19961369..19963782hg18UCSC Ensembl
Outerchr15:19960606..19964039hg18UCSC Ensembl
Innerchr15:19961369..19963782hg17UCSC Ensembl
Outerchr15:19960606..19964039hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg383434
hg193434
hg183434
hg173434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA07029
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)nssv20762
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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