A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1898e59



Internal ID20128647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57024423..57024921hg38UCSC Ensembl
chr18:54691654..54692152hg19UCSC Ensembl
chr18:52842652..52843150hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38499
hg19499
hg18499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3342486, esv3353824, esv3443071
SamplesNA19238, NA12891, NA12878
Known GenesWDR7
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1898e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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