A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6236831



Internal ID9163131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:223822..223967hg38UCSC Ensembl
chr11:223822..223967hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678621
Supporting Variants
SamplesHG01359
Known GenesSIRT3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6236831
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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