A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5868n54



Internal ID22773763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:15045812..15221737hg38UCSC Ensembl
chr18:15045811..15221736hg19UCSC Ensembl
chr18:15035811..15211736hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38175926
hg19175926
hg18175926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576544, nsv576549, nsv576547
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5868n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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