A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626878



Internal ID7013708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76961782..76966777hg38UCSC Ensembl
Innerchr11:76961818..76966742hg38UCSC Ensembl
Outerchr11:76961747..76966813hg38UCSC Ensembl
chr11:76672826..76677821hg19UCSC Ensembl
Innerchr11:76672862..76677786hg19UCSC Ensembl
Outerchr11:76672791..76677857hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384996
hg194996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214264, essv14214353, essv14214338, essv14214326, essv14214265, essv14214255, essv14214313, essv14214316, essv14214289, essv14214247, essv14214337, essv14214243, essv14214351, essv14214287, essv14214298, essv14214306, essv14214301, essv14214333, essv14214258, essv14214319, essv14214345, essv14214350, essv14214328, essv14214324, essv14214283, essv14214278, essv14214272, essv14214334, essv14214343, essv14214342, essv14214270, essv14214304, essv14214263, essv14214261, essv14214254, essv14214290, essv14214329, essv14214259, essv14214256, essv14214347, essv14214308, essv14214331, essv14214292, essv14214294, essv14214299, essv14214358, essv14214276, essv14214246, essv14214332, essv14214317, essv14214318, essv14214310, essv14214321, essv14214323, essv14214300, essv14214341, essv14214335, essv14214288, essv14214315, essv14214275, essv14214274, essv14214346, essv14214320, essv14214269, essv14214267, essv14214325, essv14214281, essv14214327, essv14214311, essv14214257, essv14214302, essv14214284, essv14214296, essv14214354, essv14214244, essv14214348, essv14214273, essv14214279, essv14214340, essv14214336, essv14214245, essv14214253, essv14214322, essv14214303, essv14214305, essv14214242, essv14214252, essv14214291, essv14214251, essv14214352, essv14214349, essv14214285, essv14214309, essv14214277, essv14214293, essv14214260, essv14214344, essv14214280, essv14214241, essv14214295, essv14214357, essv14214286, essv14214339, essv14214307, essv14214297, essv14214268, essv14214266, essv14214356, essv14214282, essv14214312, essv14214330, essv14214314, essv14214250, essv14214355, essv14214248, essv14214249, essv14214271, essv14214262
SamplesNA19701, NA19028, NA19700, HG02496, HG03484, NA19204, HG02702, HG03175, HG02433, HG03247, NA19704, NA18507, HG02337, HG02798, HG03130, HG02804, HG02476, NA18878, NA18504, HG03295, NA19314, HG02895, HG03478, HG03385, HG03452, HG03370, HG03342, HG02645, NA19197, HG03578, HG01063, NA19130, HG02981, NA19923, HG03460, HG03520, HG03556, NA18874, HG02634, NA20340, NA19238, HG02885, HG03195, HG02571, HG03380, HG02427, NA20342, HG02623, HG03114, NA19921, HG02879, HG02479, HG03343, HG02442, NA19210, HG03054, HG02554, NA19982, NA18910, HG03159, HG02470, HG02537, HG01889, NA18907, HG01390, HG03563, HG03472, HG03301, HG03085, HG02429, HG03476, HG02817, HG03397, HG03388, HG03078, HG03571, HG03451, HG02332, NA19160, HG02896, HG02568, HG02484, HG02722, HG02330, HG02807, NA19321, NA19108, NA19149, HG02983, NA19380, HG02611, HG03127, NA19428, HG02839, HG02464, HG02317, HG03557, HG03084, NA19248, HG02095, HG03025, HG02107, NA19093, NA19102, HG02013, HG03077, HG01914, HG01883, HG03445, HG02947, HG02763, NA19129, NA18488, HG02465, HG02425, HG02805, HG03439, HG03265
Known GenesACER3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626878
Frequency
Sample Size2504
Observed Gain0
Observed Loss118
Observed Complex0
Frequencyn/a


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