A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659382



Internal ID9925488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36398414..36398571hg38UCSC Ensembl
chr3:36439906..36440063hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5825466, essv6358876, essv5586024, essv6593832, essv5596880, essv6126210, essv6054934, essv6347745, essv5511987, essv6498226, essv5661249, essv5430518, essv6016780, essv6052673, essv6520427, essv6308937, essv5529454, essv5561793, essv6467773, essv5760646, essv5994170, essv6411040, essv6179379, essv5969094, essv5513847, essv5814610, essv6536157, essv5465732, essv5835509, essv5678767, essv6057308, essv5738322, essv6500632, essv6073939, essv5762707, essv5471854, essv6012633, essv5896287, essv5473114, essv6140834, essv5733743, essv5944327, essv5637266, essv6162696, essv5599479, essv5911059, essv5871743, essv6207286, essv5839622, essv6438339, essv5965954, essv6232227, essv5879355, essv5875155, essv5827030, essv5756226, essv5409138, essv6480613, essv6061941, essv6341643, essv5614821, essv6010688, essv5672091, essv5780053, essv6329970, essv5502989, essv6197040, essv5542684, essv6354772, essv5852372, essv5768556, essv5981079, essv5473083, essv6129747, essv6251639, essv6195710, essv5751278, essv5732558, essv6458466, essv6416788, essv6260553, essv5695292, essv5993527, essv6040900, essv5684378, essv6528050, essv5803426, essv5756095, essv6170878, essv5571394, essv6138717, essv6591269, essv5854000, essv5584314, essv6168467, essv5698936, essv6294530, essv5953557, essv5529746, essv6512137
SamplesHG00650, NA19397, HG00608, HG01052, HG00257, HG01066, HG00315, HG00318, HG00699, NA18530, NA18606, HG00449, HG01051, NA18633, HG00261, NA18602, HG00271, HG00663, HG01350, HG01366, HG01070, HG00251, NA18595, HG00330, NA19384, HG00537, HG00590, NA18611, NA19404, HG00139, HG01069, NA19720, HG00335, HG01072, NA19371, HG00422, HG00705, HG00309, NA18557, HG00253, HG00464, HG00108, HG00260, HG01353, HG00154, HG00268, HG00557, HG00428, NA19391, HG00436, HG00533, HG00344, HG00500, HG00263, HG00275, NA18534, HG00708, HG00284, HG01073, HG00273, HG00250, HG00479, HG00331, HG00684, HG00613, HG01334, HG00276, HG00704, HG00463, HG00246, NA18632, HG00254, HG00336, HG00285, NA18559, HG00580, HG00136, HG00473, HG00607, HG00237, NA19428, HG00319, HG01108, NA19360, HG00620, HG00672, HG00111, HG00513, HG00478, HG00421, NA18636, HG00310, HG00280, HG00252, NA18624, HG00345, NA18623, NA18612, HG00437, NA18620
Known GenesSTAC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659382
Frequency
Sample Size1151
Observed Gain0
Observed Loss100
Observed Complex0
Frequencyn/a


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