A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642887



Internal ID7029656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67010867..67069342hg38UCSC Ensembl
chr18:64678104..64736579hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3858476
hg1958476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15917540, essv15917541
SamplesHG03616, HG04141
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642887
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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