A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676155



Internal ID9942260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:35402210..35408044hg38UCSC Ensembl
Outerchr18:35402053..35408197hg38UCSC Ensembl
Innerchr18:32982174..32988008hg19UCSC Ensembl
Outerchr18:32982017..32988161hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg386145
hg196145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6038025
SamplesHG00672
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676155
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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