A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6026n54



Internal ID22773921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69033015..69088271hg38UCSC Ensembl
chr18:66700252..66755508hg19UCSC Ensembl
chr18:64851232..64906488hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3855257
hg1955257
hg1855257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577393, nsv577391
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6026n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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