A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678693



Internal ID9944798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14091178..14092152hg38UCSC Ensembl
chr3:14132678..14133652hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5576214, essv6194829, essv5790069, essv5672799, essv6395312, essv6541196, essv5592645, essv5424035, essv6574568, essv5977568, essv6274143, essv6274815, essv5605286, essv5926807, essv5678947, essv6381558, essv5963027, essv5444450, essv6475663, essv6581524, essv5964968, essv5604112, essv6261369, essv5822829, essv6097183, essv6105356, essv5803429, essv5887434, essv5577504, essv6303899, essv5592820, essv6492645, essv5584606, essv5531788, essv6337054, essv6467251, essv6175580, essv5470538, essv5977581, essv5956544, essv6340278, essv5566288, essv5395667, essv6591273, essv5890453, essv5501925, essv5534396, essv6242197, essv5639537, essv6107158, essv6467718, essv5822100, essv6359021, essv6109091, essv5485402, essv6575592, essv6289283, essv5773470, essv5874933, essv6196607, essv6400177, essv6584249, essv5652435, essv6597481, essv6305647, essv6404885, essv5745318, essv5553045, essv6427248, essv6385728, essv5731873, essv6379561, essv5998300, essv6226091, essv6400109, essv6106315, essv6552971, essv6073626, essv5538590, essv6427974, essv5654903, essv5704321, essv6119455, essv5510897, essv6214802, essv5809297, essv5953008, essv5630681, essv5707452, essv5407355, essv5479629, essv5927243, essv5774758, essv5752529, essv5856888, essv5744922, essv5580019, essv5675629, essv5555663, essv6433552, essv5700723
SamplesNA18502, NA19701, NA11830, HG01356, NA19397, NA18924, NA19909, NA19466, NA19204, NA18861, NA18508, NA19704, NA20346, NA19190, NA18870, NA19920, NA18510, NA12813, NA19396, NA19660, NA19373, NA19171, NA19379, NA19319, NA19201, NA19448, NA19119, NA18923, NA18498, NA20336, NA19904, NA19137, NA20340, NA19238, NA19385, NA19172, NA19471, NA18520, NA19445, NA20127, NA19451, NA19200, HG01124, NA19437, NA19347, NA19152, NA18933, NA18956, NA19391, NA19327, NA19236, NA18516, NA19982, HG01498, NA20126, NA19461, NA19114, HG01197, NA18499, NA18856, NA19453, NA18853, NA20282, NA19099, NA19225, NA18523, NA19160, NA19625, NA18974, NA19440, NA19390, NA11881, NA19256, NA19147, NA19435, NA19444, HG01174, NA19334, NA19470, NA19428, NA19311, HG01108, NA19376, NA18501, NA06994, NA19248, NA20334, NA19102, NA19770, NA18972, NA19900, NA19430, HG01464, NA18505, NA19129, NA18488, HG01082, NA19312, NA19463, NA19429, NA18487
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678693
Frequency
Sample Size1151
Observed Gain0
Observed Loss101
Observed Complex0
Frequencyn/a


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