A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660618



Internal ID9926723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77885698..77886925hg38UCSC Ensembl
chr5:77181522..77182749hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381228
hg191228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5539556, essv6386225, essv5786293
SamplesHG01079, HG01073, HG01107
Known GenesLOC101929154
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660618
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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