A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4614n54



Internal ID20138038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72094085..72095477hg38UCSC Ensembl
chr15:72386426..72387818hg19UCSC Ensembl
chr15:70173480..70174872hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381393
hg191393
hg181393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569939, nsv569931, nsv569930, nsv569938, nsv569934, nsv569935
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4614n54
Frequency
Sample Size17421
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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