A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569936



Internal ID16010659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094189..72095652hg38UCSC Ensembl
Innerchr15:72386530..72387993hg19UCSC Ensembl
Innerchr15:70173584..70175047hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381464
hg191464
hg181464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4613n54
Supporting Variantsnssv845064
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569936
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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