A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668168



Internal ID9587587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73986612..73991936hg38UCSC Ensembl
chr8:74898847..74904171hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg385325
hg195325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5618936, essv6517804
SamplesNA19430, NA19471
Known GenesLY96
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668168
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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