A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668422



Internal ID9587841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63272535..63273634hg38UCSC Ensembl
chr11:63040007..63041106hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6058584, essv6242940, essv5655218, essv5530158, essv6080134, essv5871152, essv6291210, essv5569394, essv5415587, essv6178697, essv6500520, essv6293219
SamplesNA19700, NA19819, HG01366, NA19372, NA19385, NA19347, NA18856, NA19625, NA19311, NA19360, NA19474, NA19346
Known GenesMIR3680-1, MIR3680-2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668422
Frequency
Sample Size1151
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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