A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669985



Internal ID9589404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1852417..1864623hg38UCSC Ensembl
Outerchr19:1852046..1864993hg38UCSC Ensembl
Innerchr19:1852416..1864622hg19UCSC Ensembl
Outerchr19:1852045..1864992hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812948
hg1912948
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
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669985
Frequency
Sample Size1151
Observed Gain0
Observed Loss97
Observed Complex0
Frequencyn/a


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