A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657844



Internal ID9923949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117121058..117121772hg38UCSC Ensembl
chr11:116991774..116992488hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6537313, essv5733580, essv5927922, essv6388913, essv5817965, essv5850157, essv5919528, essv5543539, essv5620929, essv5657420, essv5647923, essv6580034, essv6149305, essv6227993, essv5902458, essv5558870, essv6038536, essv6422936, essv6506799, essv5701671, essv5749712, essv5775051, essv5626219
SamplesHG00626, HG00592, HG00608, NA18621, HG00449, HG00654, HG00663, NA18550, NA18597, HG00689, NA18990, HG00530, HG00701, HG00436, NA18637, NA18548, NA18553, HG00463, NA18950, HG00638, HG00707, NA18987, NA18983
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657844
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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