A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5975521



Internal ID9097484
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 Flag1
Merged StatusS
Merged Variantsesv2671098
Supporting Variants
SamplesHG01080
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5975521
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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