A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6023n54



Internal ID22773918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69008880..69091760hg38UCSC Ensembl
chr18:66676117..66758997hg19UCSC Ensembl
chr18:64827097..64909977hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3882881
hg1982881
hg1882881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577384, nsv577379, nsv577385, nsv577387
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6023n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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