A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25498



Internal ID15832835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24113650..24115501hg38UCSC Ensembl
Outerchr15:24112836..24115768hg38UCSC Ensembl
Innerchr15:24358797..24360648hg19UCSC Ensembl
Outerchr15:24357983..24360915hg19UCSC Ensembl
Innerchr15:21909890..21911741hg18UCSC Ensembl
Outerchr15:21909076..21912008hg18UCSC Ensembl
Innerchr15:21909890..21911741hg17UCSC Ensembl
Outerchr15:21909076..21912008hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382933
hg192933
hg182933
hg172933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA18502
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)nssv25498
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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