A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4613n54



Internal ID20138037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72093834..72095726hg38UCSC Ensembl
chr15:72386175..72388067hg19UCSC Ensembl
chr15:70173229..70175121hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381893
hg191893
hg181893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569922, nsv569932, nsv569923, nsv569937, nsv569927, nsv569936
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4613n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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