A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642211



Internal ID7028981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35884923..35894105hg38UCSC Ensembl
Innerchr18:35884924..35894104hg38UCSC Ensembl
Outerchr18:35884922..35894106hg38UCSC Ensembl
chr18:33464886..33474068hg19UCSC Ensembl
Innerchr18:33464887..33474067hg19UCSC Ensembl
Outerchr18:33464885..33474069hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg389183
hg199183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842093, essv15842092
SamplesNA19913, HG03451
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642211
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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