A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6109396



Internal ID9086799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58226900..58292667hg38UCSC Ensembl
chr15:58519099..58584866hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3865768
hg1965768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668130
Supporting Variants
SamplesHG00531
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6109396
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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