A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22277



Internal ID15489321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34425141..34512767hg38UCSC Ensembl
Outerchr15:34424505..34513490hg38UCSC Ensembl
Innerchr15:34717342..34804968hg19UCSC Ensembl
Outerchr15:34716706..34805691hg19UCSC Ensembl
Innerchr15:32504634..32592260hg18UCSC Ensembl
Outerchr15:32503998..32592983hg18UCSC Ensembl
Innerchr15:32504634..32592260hg17UCSC Ensembl
Outerchr15:32503998..32592983hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3888986
hg1988986
hg1888986
hg1788986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA18563
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)nssv22277
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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