A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641954



Internal ID7028725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22317607..22318526hg38UCSC Ensembl
Innerchr18:22317664..22318469hg38UCSC Ensembl
Outerchr18:22317550..22318583hg38UCSC Ensembl
chr18:19897570..19898489hg19UCSC Ensembl
Innerchr18:19897627..19898432hg19UCSC Ensembl
Outerchr18:19897513..19898546hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15819468
SamplesHG00663
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641954
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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