A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642891



Internal ID7029660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67077863..67131882hg38UCSC Ensembl
chr18:64745100..64799119hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3854020
hg1954020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15917781, essv15917780
SamplesHG03616, HG04141
Known GenesMIR5011
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642891
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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