A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614460



Internal ID7001354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107532995..107535579hg38UCSC Ensembl
Innerchr7:107532996..107535579hg38UCSC Ensembl
Outerchr7:107532995..107535580hg38UCSC Ensembl
chr7:107173440..107176024hg19UCSC Ensembl
Innerchr7:107173441..107176024hg19UCSC Ensembl
Outerchr7:107173440..107176025hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg382585
hg192585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12917764, essv12917779, essv12917767, essv12917744, essv12917723, essv12917751, essv12917731, essv12917710, essv12917713, essv12917741, essv12917730, essv12917746, essv12917754, essv12917722, essv12917783, essv12917755, essv12917781, essv12917748, essv12917762, essv12917786, essv12917734, essv12917725, essv12917729, essv12917758, essv12917765, essv12917711, essv12917733, essv12917768, essv12917782, essv12917716, essv12917775, essv12917743, essv12917747, essv12917718, essv12917759, essv12917719, essv12917721, essv12917709, essv12917785, essv12917769, essv12917732, essv12917772, essv12917737, essv12917750, essv12917774, essv12917777, essv12917728, essv12917776, essv12917766, essv12917752, essv12917740, essv12917712, essv12917761, essv12917778, essv12917726, essv12917724, essv12917770, essv12917756, essv12917715, essv12917784, essv12917773, essv12917720, essv12917714, essv12917749, essv12917771, essv12917787, essv12917742, essv12917736, essv12917753, essv12917717, essv12917760, essv12917780, essv12917763, essv12917735, essv12917739, essv12917757, essv12917745, essv12917727, essv12917738
SamplesHG02944, HG02496, HG03484, NA19703, HG03378, NA19204, NA19399, HG02433, HG02337, HG03298, HG03100, NA18504, NA19377, HG03297, NA19098, NA20356, NA20359, HG03095, NA19374, HG03082, HG03099, HG03452, NA19198, HG03485, HG02756, HG03370, HG02854, HG03224, HG02816, HG02111, HG02489, HG03556, NA19024, NA19235, HG02588, HG02623, NA19025, HG03583, NA20127, HG02477, HG02479, HG02009, HG02943, NA19908, NA19210, HG03061, NA19403, NA18933, HG02449, NA18516, NA19982, NA18910, HG03081, HG02429, HG03382, HG03476, HG03078, HG01241, HG02881, HG03451, HG03046, HG01363, NA19309, NA19149, NA19454, HG03458, HG03117, NA20362, HG03103, HG03084, HG02771, NA19117, NA19223, HG03066, HG03279, HG03410, HG03118, HG03129, HG02006
Known GenesCOG5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614460
Frequency
Sample Size2504
Observed Gain0
Observed Loss79
Observed Complex0
Frequencyn/a


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