A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2669985

Internal ID9589404
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1852417..1864623hg38UCSC Ensembl
Outerchr19:1852046..1864993hg38UCSC Ensembl
Innerchr19:1852416..1864622hg19UCSC Ensembl
Outerchr19:1852045..1864992hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6065482, essv5820910, essv6452845, essv5506049, essv5593936, essv5613430, essv6043633, essv6371467, essv5801181, essv5492484, essv5976646, essv5741174, essv6184149, essv5970998, essv5873641, essv5713200, essv5933450, essv6598391, essv6423438, essv6251057, essv6390275, essv5555891, essv6053582, essv6364446, essv5433805, essv6175790, essv6162383, essv6309033, essv5551042, essv6131593, essv5923019, essv6134645, essv5516161, essv6162668, essv5596457, essv5759919, essv5629942, essv6359258, essv6045573, essv5487029, essv6013382, essv5699610, essv6132868, essv5399909, essv6093057, essv5783007, essv5836787, essv6581373, essv6573582, essv6359507, essv6580795, essv5866306, essv5939174, essv5723975, essv5528285, essv6216095, essv6111766, essv6540285, essv6468999, essv6368355, essv5564316, essv6404050, essv5448572, essv6513331, essv6176106, essv6304613, essv5740157, essv5408839, essv5878102, essv6312650, essv5991207, essv5517326, essv5654145, essv6073203, essv5557059, essv6591781, essv5486473, essv5905577, essv5860046, essv6222033, essv6133594, essv5860322, essv5537621, essv6285269, essv6104121, essv5921539, essv6418882, essv6271124, essv5667312, essv6544838, essv5536086, essv5646614, essv6408975, essv6403393, essv5821475, essv6371085, essv5610802
SamplesHG00157, HG00537, HG00252, HG00536, HG00257, HG00418, HG00100, HG00705, HG00437, HG00596, HG00131, HG00449, HG00261, HG00707, HG00463, HG00657, HG00428, HG00475, HG00542, HG00148, HG00139, HG00122, HG00106, HG00701, HG00683, HG00698, HG00581, HG00404, HG00557, HG00578, HG00146, HG00253, HG00479, HG00247, HG00256, HG00244, HG00543, HG00154, HG00158, HG00556, HG00472, HG00421, HG00140, HG00259, HG00610, HG00231, HG00141, HG00419, HG00125, HG00258, HG00634, HG00243, HG00254, HG00403, HG00237, HG00114, HG00159, HG00620, HG00124, HG00629, HG00263, HG00260, HG00239, HG00501, HG00672, HG00232, HG00249, HG00478, HG00513, HG00524, HG00512, HG00246, HG00525, HG00236, HG00120, HG00427, HG00611, HG01334, HG00118, HG00448, HG00608, HG00530, HG00708, HG00625, HG00690, HG00442, HG00473, HG00137, HG00626, HG00684, HG00143, HG00476, HG00671, HG00704, HG00136, HG00126, HG00531
Known GenesKLF16
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2669985
Sample Size1151
Observed Gain0
Observed Loss97
Observed Complex0

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