A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1473e214



Internal ID22757367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39826173..39840699hg38UCSC Ensembl
chr9:41971191..41985717hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814527
hg1914527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3620461, esv3620462
SamplesNA19394, HG01985, HG01412, HG02944, HG01918, NA21111, HG03228, HG02002, HG01443, NA20508, HG03052, NA18508, HG01031, HG03111, HG02784, HG02798, NA19350, HG03298, HG03295, HG02382, HG00115, HG03193, HG03372, HG01051, HG03603, HG03645, HG03770, HG03385, HG03808, NA18923, NA20795, HG03673, HG03874, HG03342, HG01840, NA19384, NA20291, NA11930, HG00130, HG03520, NA21109, NA20775, HG00113, NA19238, NA19207, HG03947, HG01525, HG04047, HG03585, HG00253, NA20515, NA20318, HG01565, NA12777, HG03697, NA20892, NA12760, HG01501, NA19070, NA19403, NA19175, HG02678, HG02449, NA20810, NA19455, NA19043, HG03457, HG02144, HG00344, HG03775, HG03805, HG03027, HG03781, HG01889, NA12234, NA20876, HG00740, HG03967, NA19654, NA19461, NA11919, NA20901, HG02445, NA18912, HG02259, HG01474, HG02594, HG00376, HG03934, HG03064, HG03720, NA19375, HG02330, NA19256, HG03875, HG04186, HG03949, HG01551, HG03458, HG02304, NA12873, NA20520, HG01357, HG03259, NA20902, HG02941, NA21095, NA19428, HG01620, NA12347, HG02558, HG03703, HG02771, HG01861, HG03600, HG01765, HG00513, HG00259, HG01912, NA21090, HG03977, HG03066, NA20849, NA19351, HG03279, NA20852, NA19185, HG00310, HG02013, HG03470, HG03401, HG02348, HG01111, HG04153, HG03198, HG01509, NA18612, NA11832, HG03989, HG03864, HG03741, HG03690, HG00881, HG03773, HG02339, NA18924, HG02583, NA11829, HG03731, HG02702, HG04211, HG01686, HG03100, HG01971, HG03518, NA20507, HG03139, NA18526, HG03680, NA12413, HG03074, HG03464, NA18550, HG00109, HG02151, HG03640, HG01064, HG02491, HG02485, HG02325, NA20900, HG04144, HG00736, NA19197, HG03246, NA12283, NA20540, NA19138, HG01982, HG01668, NA19651, NA19383, HG02315, HG03986, NA19137, HG01072, HG04106, HG03746, HG01892, HG03995, NA18520, NA20764, NA21114, HG04029, HG03114, NA19451, HG03270, HG03048, NA21106, NA10847, HG02009, HG01183, NA19247, NA19210, HG03054, HG01841, HG04225, NA20505, NA19152, NA19391, HG02108, HG02450, HG02307, HG01119, HG01880, HG02497, HG02537, HG01073, HG03382, HG00844, NA18499, NA19031, HG01383, HG03571, HG01705, NA19257, NA19225, HG01403, HG03755, HG03774, HG01589, NA18945, HG01990, HG01700, NA19035, NA20821, NA19308, HG02613, NA20522, NA19834, NA19108, HG02799, HG02759, HG03367, NA19473, HG03838, HG02983, HG01800, HG02923, NA12046, HG01977, HG00631, HG03433, NA19310, HG03846, NA07037, NA21126, HG03084, HG03432, HG00371, HG02974, NA19472, HG03863, HG00656, HG02938, HG01055, HG01085, HG00234, HG01105, HG03445, NA18505, HG03882, HG01775, NA18488, HG01566, NA07000, HG03129, HG02343, HG03686
Known GenesKGFLP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1473e214
Frequency
Sample Size2504
Observed Gain279
Observed Loss0
Observed Complex0
Frequencyn/a


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