A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25099



Internal ID15839647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28651599..28653227hg38UCSC Ensembl
Outerchr15:28651125..28653819hg38UCSC Ensembl
Innerchr15:28896745..28898373hg19UCSC Ensembl
Outerchr15:28896271..28898965hg19UCSC Ensembl
Innerchr15:26695786..26697414hg18UCSC Ensembl
Outerchr15:26695312..26698006hg18UCSC Ensembl
Innerchr15:26695786..26697414hg17UCSC Ensembl
Outerchr15:26695312..26698006hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382695
hg192695
hg182695
hg172695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9216
Supporting Variants
SamplesNA18972
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)nssv25099
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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