A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637117



Internal ID7023911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85521579..85639396hg38UCSC Ensembl
chr15:86064810..86182627hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38117818
hg19117818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15315386, essv15315361, essv15315393, essv15315484, essv15315464, essv15315446, essv15315403, essv15315486, essv15315423, essv15315487, essv15315374, essv15315394, essv15315471, essv15315383, essv15315362, essv15315482, essv15315417, essv15315458, essv15315473, essv15315365, essv15315432, essv15315416, essv15315400, essv15315390, essv15315437, essv15315363, essv15315380, essv15315444, essv15315443, essv15315351, essv15315466, essv15315354, essv15315472, essv15315376, essv15315427, essv15315375, essv15315434, essv15315439, essv15315435, essv15315414, essv15315410, essv15315485, essv15315470, essv15315449, essv15315421, essv15315459, essv15315408, essv15315409, essv15315436, essv15315475, essv15315418, essv15315426, essv15315391, essv15315465, essv15315453, essv15315445, essv15315457, essv15315483, essv15315448, essv15315382, essv15315456, essv15315440, essv15315381, essv15315431, essv15315450, essv15315397, essv15315398, essv15315452, essv15315406, essv15315481, essv15315360, essv15315387, essv15315368, essv15315428, essv15315370, essv15315385, essv15315377, essv15315424, essv15315388, essv15315355, essv15315478, essv15315451, essv15315389, essv15315359, essv15315422, essv15315447, essv15315373, essv15315488, essv15315413, essv15315420, essv15315364, essv15315412, essv15315463, essv15315399, essv15315395, essv15315455, essv15315371, essv15315415, essv15315407, essv15315379, essv15315469, essv15315477, essv15315419, essv15315479, essv15315454, essv15315402, essv15315352, essv15315430, essv15315468, essv15315366, essv15315429, essv15315392, essv15315433, essv15315369, essv15315476, essv15315396, essv15315353, essv15315461, essv15315467, essv15315480, essv15315474, essv15315442, essv15315405, essv15315441, essv15315425, essv15315462, essv15315411, essv15315384, essv15315401, essv15315357, essv15315404, essv15315372, essv15315356, essv15315460, essv15315367, essv15315378, essv15315358, essv15315438
SamplesHG01060, HG03773, HG00235, HG01412, HG01918, HG01961, NA21099, HG02784, HG02262, HG04202, HG03738, HG02150, HG03717, HG02727, HG01970, HG04094, HG02600, HG03772, HG04018, HG03229, HG01456, NA20332, HG01971, HG03895, HG02734, HG02688, HG01051, HG03944, HG03950, HG03680, HG01325, HG03770, HG03016, HG01953, HG03943, HG03490, HG02491, HG03873, HG02687, HG01968, HG03673, HG03629, HG03479, HG02733, HG02786, HG03868, HG03897, HG03624, HG03947, HG01176, HG01973, HG04238, HG04047, HG03744, HG01967, HG03784, NA18648, HG02737, HG03844, HG03780, HG02439, HG03861, HG01435, HG01187, HG03644, HG02697, HG03760, HG03786, HG01095, HG04107, HG01088, HG03711, HG02775, HG03771, HG03775, HG04019, HG02728, HG01077, HG03756, HG03781, HG03021, HG02789, HG01092, HG03742, HG01392, HG01311, HG03871, HG03858, HG03713, HG02787, HG02657, HG01613, HG03643, HG04017, HG01101, HG04063, HG03634, HG02783, HG02724, HG02601, HG02725, HG03991, HG03653, HG03238, HG02660, HG02455, HG03848, HG02557, HG01954, HG00742, HG04239, HG02696, HG01878, HG02790, HG03695, HG01977, HG03702, HG03488, HG01974, HG04003, HG03779, HG04080, HG04023, HG02700, HG02128, HG04015, HG03789, HG03642, HG03849, HG03022, HG03998, HG03716, HG03882, HG02778, HG03890, HG01886, NA21104, HG03864
Known GenesAKAP13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637117
Frequency
Sample Size2504
Observed Gain0
Observed Loss138
Observed Complex0
Frequencyn/a


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