A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27333



Internal ID15497176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30435153..30469780hg38UCSC Ensembl
Outerchr15:30435053..30469995hg38UCSC Ensembl
Innerchr15:30727356..30761983hg19UCSC Ensembl
Outerchr15:30727256..30762198hg19UCSC Ensembl
Innerchr15:28514648..28549275hg18UCSC Ensembl
Outerchr15:28514548..28549490hg18UCSC Ensembl
Innerchr15:28514648..28549275hg17UCSC Ensembl
Outerchr15:28514548..28549490hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3834943
hg1934943
hg1834943
hg1734943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9232
Supporting Variants
SamplesNA19221
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)nssv27333
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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