A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643158



Internal ID7029927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76080534..76090732hg38UCSC Ensembl
Innerchr18:76080534..76090732hg38UCSC Ensembl
Outerchr18:76080034..76091232hg38UCSC Ensembl
chr18:73792489..73802687hg19UCSC Ensembl
Innerchr18:73792489..73802687hg19UCSC Ensembl
Outerchr18:73791989..73803187hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3810199
hg1910199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15936298, essv15936299, essv15936300
SamplesNA06984, HG03061, HG03743
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643158
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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