A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6004n54



Internal ID22773899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:66903284..67004349hg38UCSC Ensembl
chr18:64570521..64671586hg19UCSC Ensembl
chr18:62721501..62822566hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38101066
hg19101066
hg18101066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577284, nsv577285
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6004n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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