A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665572



Internal ID9931677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1522128..1522902hg38UCSC Ensembl
chr11:1543358..1544132hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6366958, essv5471832, essv6495165, essv6283593, essv6490242, essv5542779, essv5757165, essv6331051, essv5914093, essv5764807, essv6487592, essv5488062, essv6366978
SamplesNA19703, NA19204, NA18486, NA18519, NA19172, NA18867, NA18499, NA18912, NA18853, NA19160, NA19108, NA19398, NA19472
Known GenesMOB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665572
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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