A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5952555



Internal ID9313396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89724788..89728692hg38UCSC Ensembl
chr8:90737016..90740920hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg383905
hg193905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676328
Supporting Variants
SamplesNA18504
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5952555
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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