A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625614



Internal ID7012448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22285555..22292049hg38UCSC Ensembl
Innerchr11:22285610..22291995hg38UCSC Ensembl
Outerchr11:22285501..22292104hg38UCSC Ensembl
chr11:22307101..22313595hg19UCSC Ensembl
Innerchr11:22307156..22313541hg19UCSC Ensembl
Outerchr11:22307047..22313650hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg386495
hg196495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14050088, essv14050079, essv14050087, essv14050075, essv14050107, essv14050082, essv14050099, essv14050102, essv14050084, essv14050085, essv14050095, essv14050106, essv14050076, essv14050098, essv14050101, essv14050090, essv14050091, essv14050104, essv14050103, essv14050096, essv14050074, essv14050100, essv14050073, essv14050083, essv14050078, essv14050105, essv14050093, essv14050092, essv14050081, essv14050094, essv14050080, essv14050077, essv14050072, essv14050097, essv14050089, essv14050086
SamplesHG02610, HG03121, HG03378, NA19466, NA19020, HG00640, HG03280, HG03464, HG03209, HG03460, NA19383, NA18874, HG03045, HG02642, HG03352, NA19451, HG01256, NA19327, HG01383, HG01241, HG03024, NA19452, NA19160, NA19095, NA19395, NA18909, HG02721, HG03304, NA20357, NA19713, HG03258, HG02763, HG02855, NA19312, HG02629, NA19346
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625614
Frequency
Sample Size2504
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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