A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628109



Internal ID6668253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131726291..131727357hg38UCSC Ensembl
Innerchr11:131726300..131727348hg38UCSC Ensembl
Outerchr11:131726282..131727366hg38UCSC Ensembl
chr11:131596185..131597251hg19UCSC Ensembl
Innerchr11:131596194..131597242hg19UCSC Ensembl
Outerchr11:131596176..131597260hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381067
hg191067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14316965, essv14317029, essv14316983, essv14317089, essv14317038, essv14317040, essv14316979, essv14316986, essv14316996, essv14317037, essv14316981, essv14317063, essv14317070, essv14317025, essv14317084, essv14317065, essv14316993, essv14316971, essv14317039, essv14317043, essv14316977, essv14317011, essv14316999, essv14317047, essv14317069, essv14316964, essv14317023, essv14317064, essv14317026, essv14317078, essv14317008, essv14317031, essv14317003, essv14317006, essv14316975, essv14317068, essv14317045, essv14316994, essv14317015, essv14317050, essv14316972, essv14317087, essv14317044, essv14317077, essv14317061, essv14317082, essv14317056, essv14316976, essv14317004, essv14316980, essv14316992, essv14317033, essv14317042, essv14316968, essv14317034, essv14316991, essv14317001, essv14317014, essv14317032, essv14317027, essv14316969, essv14317051, essv14316967, essv14317052, essv14317066, essv14316963, essv14317016, essv14317059, essv14317075, essv14316974, essv14317036, essv14317048, essv14317041, essv14317067, essv14317007, essv14317083, essv14316978, essv14316982, essv14317072, essv14316966, essv14317049, essv14317081, essv14317055, essv14317080, essv14317002, essv14317088, essv14317010, essv14316987, essv14317062, essv14317054, essv14317057, essv14317035, essv14317053, essv14317018, essv14316997, essv14316962, essv14317013, essv14317019, essv14316998, essv14316990, essv14317021, essv14317074, essv14316995, essv14316985, essv14317022, essv14317071, essv14317028, essv14317024, essv14316973, essv14317086, essv14317012, essv14317079, essv14317085, essv14316989, essv14317017, essv14317090, essv14317000, essv14316970, essv14317060, essv14316984, essv14317046, essv14317009, essv14317005, essv14317020, essv14317073, essv14317058, essv14316988, essv14317076, essv14317030
SamplesHG02890, NA19146, NA19913, NA19312, HG03120, NA19904, HG02970, HG03382, HG01896, NA18871, NA19222, HG01988, HG02546, HG01882, HG03563, HG03437, HG03410, NA19093, HG02549, HG03055, HG03066, HG03129, HG01885, HG02255, NA19023, HG03247, HG03295, NA19455, NA19435, NA18517, HG02722, HG02885, HG03124, HG02884, HG02508, HG02314, HG03458, HG03099, HG03401, HG02817, NA19108, HG03485, HG02323, HG03380, NA19236, HG03378, NA19308, NA19043, HG02836, HG02982, NA19028, HG02981, HG03461, HG03470, NA19323, HG01392, HG02646, HG02716, NA19471, HG03439, NA18856, HG03464, HG03520, HG03130, HG03024, HG03100, HG01879, HG03027, NA19042, NA19213, HG01242, NA19247, HG02814, NA19377, NA19395, HG02442, NA19172, NA20291, NA19384, NA18498, HG02461, HG02922, HG02594, HG03472, NA19713, NA19901, HG02558, HG02611, HG02343, HG02938, HG02111, HG03518, NA19909, HG03072, HG02502, HG03297, HG03118, HG02339, HG03175, HG03352, HG03446, HG01405, NA20332, HG03045, HG03246, NA20289, NA19099, HG03476, NA18864, HG03240, HG03081, HG02465, HG01366, HG02256, HG03369, HG03139, HG03270, NA19118, HG02721, HG03060, NA19204, NA19113, NA20804, HG02051, HG02574, HG01890, NA18881, NA19385, HG02282
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628109
Frequency
Sample Size2504
Observed Gain0
Observed Loss129
Observed Complex0
Frequencyn/a


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