A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6099n54



Internal ID22773994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78978993..78980923hg38UCSC Ensembl
chr18:76738993..76740923hg19UCSC Ensembl
chr18:74839981..74841911hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381931
hg191931
hg181931
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577797, nsv577798
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6099n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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