A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9829n54



Internal ID22777724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66665153..66768198hg38UCSC Ensembl
chr5:65960981..66064026hg19UCSC Ensembl
chr5:65996737..66099782hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38103046
hg19103046
hg18103046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598406, nsv598405
Samples
Known GenesMAST4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9829n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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