A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26607



Internal ID15834184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55762591..55788449hg38UCSC Ensembl
Outerchr16:55762006..55788975hg38UCSC Ensembl
Innerchr16:55796503..55822361hg19UCSC Ensembl
Outerchr16:55795918..55822887hg19UCSC Ensembl
Innerchr16:54354004..54379862hg18UCSC Ensembl
Outerchr16:54353419..54380388hg18UCSC Ensembl
Innerchr16:54354004..54379862hg17UCSC Ensembl
Outerchr16:54353419..54380388hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3826970
hg1926970
hg1826970
hg1726970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9445
Supporting Variants
SamplesNA18517
Known GenesCES1P1
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)nssv26607
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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