A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6491406



Internal ID9080908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73499175..73515252hg38UCSC Ensembl
chr15:73791516..73807593hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3816078
hg1916078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673071
Supporting Variants
SamplesHG01060
Known GenesC15orf60
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6491406
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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