A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5964n54



Internal ID22773859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62039466..62044077hg38UCSC Ensembl
chr18:59706699..59711310hg19UCSC Ensembl
chr18:57857679..57862290hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg384612
hg194612
hg184612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577079, nsv577078
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5964n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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