A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626558



Internal ID7013390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60460477..60461927hg38UCSC Ensembl
Innerchr11:60460491..60461913hg38UCSC Ensembl
Outerchr11:60460463..60461941hg38UCSC Ensembl
chr11:60227950..60229400hg19UCSC Ensembl
Innerchr11:60227964..60229386hg19UCSC Ensembl
Outerchr11:60227936..60229414hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381451
hg191451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14174992, essv14174963, essv14175019, essv14175059, essv14175048, essv14174998, essv14175055, essv14175057, essv14174975, essv14175050, essv14175038, essv14174969, essv14174962, essv14175007, essv14175000, essv14175005, essv14175026, essv14175040, essv14175013, essv14175046, essv14175022, essv14175021, essv14174994, essv14175024, essv14174996, essv14174979, essv14175014, essv14175025, essv14175049, essv14174997, essv14175058, essv14174990, essv14174964, essv14174968, essv14175018, essv14174984, essv14174989, essv14175056, essv14174982, essv14175015, essv14175020, essv14174999, essv14174985, essv14175009, essv14174966, essv14175016, essv14174971, essv14175053, essv14175012, essv14175039, essv14174972, essv14174995, essv14174978, essv14175054, essv14175030, essv14175052, essv14175037, essv14175045, essv14174991, essv14175006, essv14174987, essv14174977, essv14175029, essv14175036, essv14175033, essv14175035, essv14175034, essv14174970, essv14175023, essv14174965, essv14175041, essv14174980, essv14175031, essv14174983, essv14174961, essv14175047, essv14175011, essv14175002, essv14175044, essv14175028, essv14174967, essv14174993, essv14174960, essv14175004, essv14174976, essv14175003, essv14175042, essv14175008, essv14174981, essv14175010, essv14174974, essv14175017, essv14175027, essv14174988, essv14174986, essv14175001, essv14175051, essv14175043, essv14175032, essv14174973
SamplesHG00626, NA18998, HG01413, HG00650, HG01402, HG01098, HG01918, HG01054, HG01462, HG01961, HG02262, HG01326, NA18599, HG01970, HG00457, HG02277, HG03229, NA21137, NA19684, HG02271, HG02040, HG02285, HG01924, HG01571, HG01250, NA19746, HG01350, HG01953, HG02407, NA19728, HG01351, NA18595, HG01277, HG01459, HG02266, HG01945, HG00537, HG03619, HG01308, HG01176, HG02104, HG01844, HG01275, NA19007, NA18605, HG02265, HG01360, HG00982, HG01247, NA19077, HG02076, HG01938, HG01979, HG00556, HG00500, HG01447, HG00690, HG02259, HG01101, NA18553, HG01497, NA19009, HG02408, NA18541, NA18546, HG01363, NA19729, HG00476, HG01597, NA18543, NA18559, HG01551, HG00734, HG02304, HG01272, NA19773, HG01598, HG02179, HG01933, NA19783, HG02019, NA18615, HG01489, HG02401, HG01917, HG02367, HG02147, HG01935, HG01254, HG01269, HG01817, HG00698, HG02291, HG01251, NA19661, HG01807, HG01464, HG01111, HG01191, HG01926
Known GenesMS4A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626558
Frequency
Sample Size2504
Observed Gain0
Observed Loss100
Observed Complex0
Frequencyn/a


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