A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5988872



Internal ID9068212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127815696..127816181hg38UCSC Ensembl
chr11:127685591..127686076hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658104
Supporting Variants
SamplesHG00736
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5988872
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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