A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620468



Internal ID7007339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66769053..66782333hg38UCSC Ensembl
chr9:43450178..43463455hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3813281
hg1913278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1475e214
Supporting Variantsessv13476335, essv13476363, essv13476343, essv13476330, essv13476336, essv13476414, essv13476374, essv13476360, essv13476393, essv13476357, essv13476339, essv13476424, essv13476389, essv13476326, essv13476427, essv13476434, essv13476317, essv13476405, essv13476435, essv13476400, essv13476359, essv13476416, essv13476418, essv13476392, essv13476398, essv13476364, essv13476408, essv13476376, essv13476366, essv13476367, essv13476443, essv13476406, essv13476352, essv13476371, essv13476354, essv13476441, essv13476410, essv13476401, essv13476318, essv13476321, essv13476429, essv13476431, essv13476422, essv13476387, essv13476381, essv13476355, essv13476430, essv13476365, essv13476338, essv13476353, essv13476383, essv13476342, essv13476388, essv13476423, essv13476390, essv13476437, essv13476391, essv13476340, essv13476316, essv13476345, essv13476420, essv13476328, essv13476411, essv13476412, essv13476369, essv13476425, essv13476341, essv13476439, essv13476331, essv13476323, essv13476356, essv13476413, essv13476332, essv13476421, essv13476419, essv13476377, essv13476327, essv13476403, essv13476370, essv13476337, essv13476428, essv13476347, essv13476320, essv13476358, essv13476396, essv13476385, essv13476346, essv13476325, essv13476404, essv13476344, essv13476350, essv13476372, essv13476379, essv13476378, essv13476349, essv13476409, essv13476368, essv13476329, essv13476348, essv13476324, essv13476397, essv13476380, essv13476319, essv13476436, essv13476386, essv13476433, essv13476442, essv13476417, essv13476362, essv13476415, essv13476334, essv13476322, essv13476361, essv13476407, essv13476382, essv13476399, essv13476440, essv13476426, essv13476351, essv13476432, essv13476384, essv13476438, essv13476394, essv13476375, essv13476333, essv13476402, essv13476373, essv13476395
SamplesHG01746, NA21097, NA12842, NA18947, HG01438, NA20508, NA11995, HG01885, HG01348, HG00351, HG01079, HG02648, HG03300, NA18979, HG02804, NA12340, NA12058, HG00179, HG01632, HG00337, HG00271, NA12813, NA20814, NA20796, HG03770, HG02140, HG00689, NA20795, HG00458, NA12348, HG03736, NA11918, HG02374, HG00346, NA12762, NA12287, NA20287, HG00185, HG02816, HG00158, HG03793, HG02281, NA11930, HG00139, NA20759, HG00277, NA20278, NA20775, HG00309, HG00118, HG02946, HG02104, HG00338, HG01771, HG02780, HG00326, HG02882, NA20318, NA20753, HG02879, HG00133, HG00188, NA20800, HG03132, HG01867, HG01171, HG00380, NA19006, HG00332, HG01247, HG04162, HG02775, HG01810, HG00533, HG00344, HG04035, HG01077, HG01852, HG04177, HG01161, NA19000, HG00250, NA11893, NA18532, HG04063, NA18555, HG01474, HG01708, HG00099, HG04118, HG00240, HG02330, HG00476, HG03866, HG00155, HG00254, HG00119, HG00336, NA19019, HG00742, HG04239, HG02696, HG02220, HG00375, HG01685, NA20351, NA20530, NA20527, HG03850, HG01620, HG02464, NA12874, NA12763, NA18971, HG02095, HG03896, HG03849, NA12749, HG02079, HG03684, HG02768, HG01431, HG01464, NA12006, HG01672, NA18740, HG01112, HG01578
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620468
Frequency
Sample Size2504
Observed Gain128
Observed Loss0
Observed Complex0
Frequencyn/a


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