A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671098



Internal ID9937203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26938850..27061756hg38UCSC Ensembl
chr8:26796367..26919273hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38122907
hg19122907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5975521, essv5713156
SamplesHG01080, HG00160
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671098
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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