A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642979



Internal ID6683059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69876494..69891905hg38UCSC Ensembl
chr18:67543730..67559141hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3815412
hg1915412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv632e214
Supporting Variantsessv15930777, essv15930776
SamplesNA06984, HG03947
Known GenesCD226
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642979
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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