A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626736



Internal ID6666884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68299773..68301695hg38UCSC Ensembl
Innerchr11:68299804..68301665hg38UCSC Ensembl
Outerchr11:68299743..68301726hg38UCSC Ensembl
chr11:68067241..68069163hg19UCSC Ensembl
Innerchr11:68067272..68069133hg19UCSC Ensembl
Outerchr11:68067211..68069194hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381923
hg191923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14200249, essv14200169, essv14200139, essv14200133, essv14200272, essv14200158, essv14200096, essv14200219, essv14200127, essv14200266, essv14200097, essv14200227, essv14200263, essv14200237, essv14200159, essv14200090, essv14200276, essv14200087, essv14200198, essv14200185, essv14200112, essv14200204, essv14200130, essv14200277, essv14200109, essv14200282, essv14200148, essv14200099, essv14200229, essv14200274, essv14200248, essv14200234, essv14200152, essv14200110, essv14200228, essv14200215, essv14200232, essv14200125, essv14200115, essv14200078, essv14200176, essv14200177, essv14200209, essv14200153, essv14200077, essv14200192, essv14200123, essv14200205, essv14200156, essv14200218, essv14200199, essv14200145, essv14200213, essv14200223, essv14200222, essv14200164, essv14200238, essv14200252, essv14200196, essv14200162, essv14200180, essv14200107, essv14200224, essv14200260, essv14200171, essv14200253, essv14200184, essv14200217, essv14200251, essv14200155, essv14200175, essv14200207, essv14200191, essv14200146, essv14200163, essv14200073, essv14200194, essv14200134, essv14200261, essv14200135, essv14200236, essv14200206, essv14200195, essv14200278, essv14200270, essv14200140, essv14200142, essv14200117, essv14200281, essv14200101, essv14200262, essv14200187, essv14200174, essv14200161, essv14200094, essv14200243, essv14200212, essv14200114, essv14200168, essv14200271, essv14200143, essv14200118, essv14200104, essv14200241, essv14200203, essv14200264, essv14200245, essv14200190, essv14200116, essv14200279, essv14200275, essv14200165, essv14200082, essv14200100, essv14200230, essv14200197, essv14200239, essv14200170, essv14200221, essv14200257, essv14200200, essv14200186, essv14200091, essv14200240, essv14200268, essv14200149, essv14200124, essv14200247, essv14200254, essv14200183, essv14200093, essv14200106, essv14200267, essv14200265, essv14200105, essv14200201, essv14200075, essv14200225, essv14200211, essv14200089, essv14200080, essv14200144, essv14200092, essv14200083, essv14200157, essv14200193, essv14200088, essv14200138, essv14200189, essv14200122, essv14200246, essv14200129, essv14200121, essv14200231, essv14200255, essv14200126, essv14200256, essv14200220, essv14200166, essv14200150, essv14200108, essv14200188, essv14200074, essv14200102, essv14200202, essv14200079, essv14200280, essv14200132, essv14200250, essv14200120, essv14200179, essv14200085, essv14200095, essv14200259, essv14200210, essv14200103, essv14200131, essv14200269, essv14200173, essv14200258, essv14200244, essv14200167, essv14200160, essv14200182, essv14200208, essv14200273, essv14200113, essv14200226, essv14200172, essv14200216, essv14200242, essv14200151, essv14200086, essv14200111, essv14200076, essv14200081, essv14200181, essv14200178, essv14200147, essv14200128, essv14200137, essv14200119, essv14200233, essv14200154, essv14200141, essv14200098, essv14200084, essv14200235, essv14200214, essv14200136
SamplesNA07000, HG01112, HG01695, HG00553, NA11832, HG00255, NA19676, HG03989, HG01516, NA20511, HG00096, HG01485, HG00189, HG00235, NA19648, HG01402, HG02496, HG02652, HG01098, HG01356, HG01303, HG00102, NA12286, HG01624, HG00384, HG00351, HG01079, HG01280, NA20531, NA11933, HG01066, HG00151, NA20532, NA20512, HG00318, HG00244, HG00181, HG01686, HG01531, HG03018, HG01947, HG00150, NA20517, NA12155, NA20806, HG01694, HG01513, HG00337, HG00327, NA12813, HG00138, NA12812, HG00251, HG01953, HG01702, NA20798, HG02105, HG01676, HG00173, NA20756, NA18619, HG01459, NA12348, HG01492, NA11992, HG00346, NA12287, HG01083, HG00334, NA19681, HG01982, HG01668, HG01393, HG01242, NA12761, HG01134, NA12275, HG04183, NA20819, HG01628, HG01519, HG00236, HG00325, NA19917, NA11932, HG00113, HG03691, NA12889, NA12815, HG01525, HG00182, HG03744, HG00160, HG01275, NA20587, HG00253, NA20753, NA12748, HG01256, HG01524, NA11831, HG01353, HG00349, HG00137, NA12777, HG01183, HG00290, HG00154, NA12760, NA12489, HG01248, HG00183, HG01501, HG01435, HG00380, HG02233, HG01122, NA20524, HG01384, HG02345, NA12342, HG02334, HG00360, NA20885, HG04107, HG01515, HG00101, HG03928, HG01879, HG02108, HG02554, NA20895, HG02731, HG00320, HG01768, HG00344, NA21118, NA21098, NA19658, NA20832, HG02221, HG01630, HG01047, HG01777, HG00250, HG01536, NA12249, HG04189, HG01130, HG01497, HG01705, HG02725, NA12144, HG01403, NA20828, HG01286, HG04159, HG00099, NA12778, HG02219, HG03774, NA20542, NA12546, NA20534, HG01700, HG01257, HG01148, NA20851, HG00382, NA20773, HG04219, NA20801, HG00336, HG00265, NA19749, HG01678, HG00375, HG01685, HG01362, HG00136, HG02651, HG01375, HG01494, HG01620, HG01137, HG00116, NA06986, HG00125, NA19759, NA20906, HG00111, HG01765, HG01770, HG02238, HG00329, HG00288, HG01302, HG01085, HG00123, NA12830, HG00310, HG00186, HG01631, HG00343, HG00105, HG01617, HG01756, NA11892, HG01378, HG00345
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626736
Frequency
Sample Size2504
Observed Gain0
Observed Loss210
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer