A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6101n54



Internal ID20139525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78979457..78980923hg38UCSC Ensembl
chr18:76739457..76740923hg19UCSC Ensembl
chr18:74840445..74841911hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381467
hg191467
hg181467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577813, nsv577809, nsv577802, nsv577804, nsv577807
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6101n54
Frequency
Sample Size17421
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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