A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5963n54



Internal ID22773858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62039466..62040252hg38UCSC Ensembl
chr18:59706699..59707485hg19UCSC Ensembl
chr18:57857679..57858465hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38787
hg19787
hg18787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577075, nsv577080, nsv577076, nsv577077
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5963n54
Frequency
Sample Size17421
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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