A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6571063



Internal ID9548467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112022547..112024925hg38UCSC Ensembl
chr11:111893271..111895649hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382379
hg192379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662119
Supporting Variants
SamplesNA19379
Known GenesDIXDC1, DLAT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6571063
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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