A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642783



Internal ID7029552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63811664..63845279hg38UCSC Ensembl
chr18:61478898..61512513hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3833616
hg1933616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv622e214
Supporting Variantsessv15906740, essv15906739
SamplesHG04035, HG03702
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642783
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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