A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569133



Internal ID16009856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34589103..34850365hg38UCSC Ensembl
Innerchr15:34881304..35142566hg19UCSC Ensembl
Innerchr15:32668596..32929858hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38261263
hg19261263
hg18261263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840395
Samples
Known GenesACTC1, GJD2, MIR5588
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569133
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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