A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6240955



Internal ID9099872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123808260..123811091hg38UCSC Ensembl
chr11:123678968..123681799hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382832
hg192832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667746
Supporting Variants
SamplesHG01082
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6240955
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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