A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4925n54



Internal ID20138349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15856272..15856939hg38UCSC Ensembl
chr16:15950129..15950796hg19UCSC Ensembl
chr16:15857630..15858297hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38668
hg19668
hg18668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571539, nsv571541, nsv571540
Samples
Known GenesMYH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4925n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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