A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5966n54



Internal ID20139390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62522582..62525061hg38UCSC Ensembl
chr18:60189815..60192294hg19UCSC Ensembl
chr18:58340795..58343274hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg382480
hg192480
hg182480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577090, nsv577088
Samples
Known GenesZCCHC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5966n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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