A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569934



Internal ID16010657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094189..72095338hg38UCSC Ensembl
Innerchr15:72386530..72387679hg19UCSC Ensembl
Innerchr15:70173584..70174733hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381150
hg191150
hg181150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4614n54
Supporting Variantsnssv845056, nssv845062, nssv845054, nssv845055, nssv845059, nssv845061, nssv845057, nssv845058, nssv845060
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569934
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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