A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1927e59



Internal ID22763147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75864509..75865607hg38UCSC Ensembl
chr18:73576464..73577562hg19UCSC Ensembl
chr18:71705452..71706550hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3357759, esv3435049
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1927e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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