A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642680



Internal ID7029449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59943092..59947383hg38UCSC Ensembl
Innerchr18:59943242..59947233hg38UCSC Ensembl
Outerchr18:59942942..59947533hg38UCSC Ensembl
chr18:57610324..57614615hg19UCSC Ensembl
Innerchr18:57610474..57614465hg19UCSC Ensembl
Outerchr18:57610174..57614765hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg384292
hg194292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15897373
SamplesHG03280
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642680
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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