A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668259



Internal ID9934364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23159526..23161337hg38UCSC Ensembl
chr6:23159754..23161565hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5650847, essv6281993, essv6461018, essv5595554, essv6381566, essv6508707
SamplesNA19394, NA18870, NA19360, NA19818, NA19713, NA19711
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668259
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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