A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21474



Internal ID15840063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28267573..28271710hg38UCSC Ensembl
Outerchr15:28265746..28272149hg38UCSC Ensembl
Innerchr15:28512719..28516856hg19UCSC Ensembl
Outerchr15:28510892..28517295hg19UCSC Ensembl
Innerchr15:26186314..26190451hg18UCSC Ensembl
Outerchr15:26184487..26190890hg18UCSC Ensembl
Innerchr15:26186314..26190451hg17UCSC 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 StatusS
Merged Variantsnsv9207
Supporting Variants
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)nssv21474
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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