A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6110888



Internal ID8727599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67739401..67968312hg38UCSC Ensembl
chr11:67506872..67735783hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38228912
hg19228912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678476
Supporting Variants
SamplesHG00113
Known GenesFAM86C2P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6110888
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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