A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21976



Internal ID15488907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34536586..34549988hg38UCSC Ensembl
Outerchr15:34535791..34551848hg38UCSC Ensembl
Innerchr15:34828787..34842189hg19UCSC Ensembl
Outerchr15:34827992..34844049hg19UCSC Ensembl
Innerchr15:32616079..32629481hg18UCSC Ensembl
Outerchr15:32615284..32631341hg18UCSC Ensembl
Innerchr15:32616079..32629481hg17UCSC Ensembl
Outerchr15:32615284..32631341hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3816058
hg1916058
hg1816058
hg1716058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA18552
Known GenesGOLGA8B
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)nssv21976
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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