A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674139



Internal ID9940244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166052616..166055808hg38UCSC Ensembl
chr6:166466104..166469296hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383193
hg193193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6287057
SamplesNA18516
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674139
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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