A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9207



Internal ID15847119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28265746..28272149hg38UCSC Ensembl
Outerchr15:28510892..28517295hg19UCSC Ensembl
Outerchr15:26184487..26190890hg18UCSC Ensembl
Outerchr15:26184487..26190890hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg386404
hg196404
hg186404
hg176404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21474
SamplesNA18975
Known GenesHERC2
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)nsv9207
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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