A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22863



Internal ID15484831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34436507..34517676hg38UCSC Ensembl
Outerchr15:34435461..34520188hg38UCSC Ensembl
Innerchr15:34728708..34809877hg19UCSC Ensembl
Outerchr15:34727662..34812389hg19UCSC Ensembl
Innerchr15:32516000..32597169hg18UCSC Ensembl
Outerchr15:32514954..32599681hg18UCSC Ensembl
Innerchr15:32516000..32597169hg17UCSC Ensembl
Outerchr15:32514954..32599681hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3884728
hg1984728
hg1884728
hg1784728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA12740
Known GenesGOLGA8A
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)nssv22863
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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