A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv622e214



Internal ID22756516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63810723..63845279hg38UCSC Ensembl
chr18:61477957..61512513hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3834557
hg1934557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3642783, esv3642782
SamplesHG04035, HG03702
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv622e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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