A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5680219



Internal ID9142424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65805555..65811314hg38UCSC Ensembl
chr15:66097893..66103652hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385760
hg195760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677148
Supporting Variants
SamplesHG01190
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5680219
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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