A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6036n54



Internal ID22773931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69078971..69145197hg38UCSC Ensembl
chr18:66746208..66812434hg19UCSC Ensembl
chr18:64897188..64963414hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3866227
hg1966227
hg1866227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577481, nsv577430
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6036n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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