A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6291210



Internal ID9268613
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 Flag1
Merged StatusS
Merged Variantsesv2668422
Supporting Variants
SamplesNA18856
Known GenesMIR3680-1, MIR3680-2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6291210
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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