A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658124



Internal ID9924229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128054361..128065525hg38UCSC Ensembl
chr11:127924256..127935420hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3811165
hg1911165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6457617
SamplesHG00607
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658124
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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