A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9218



Internal ID15847130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28675599..28680998hg38UCSC Ensembl
Outerchr15:28920745..28926144hg19UCSC Ensembl
Outerchr15:26719786..26725185hg18UCSC Ensembl
Outerchr15:26719786..26725185hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg385400
hg195400
hg185400
hg175400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25755
SamplesNA18502
Known GenesHERC2P9
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)nsv9218
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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