A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5961n54



Internal ID22773856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60600610..60649293hg38UCSC Ensembl
chr18:58267843..58316526hg19UCSC Ensembl
chr18:56418823..56467506hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3848684
hg1948684
hg1848684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577069, nsv577070, nsv577068
Samples1782681110_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5961n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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