A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659362



Internal ID9925467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41361547..41361898hg38UCSC Ensembl
chr19:41867452..41867803hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5993905, essv6265218, essv6173135, essv5834501, essv5570544, essv5948882, essv6276404, essv5592460, essv5753460, essv6054969, essv5580722, essv6218548, essv6494355, essv5915397, essv5477017, essv5758267, essv6085269, essv6008329, essv5985759, essv5701606, essv6210421, essv6403104, essv6094676, essv5430096, essv5400228, essv5688327, essv6097859, essv5418854, essv6472173, essv6032783, essv6481298, essv6274341, essv5496760, essv5519663, essv5960196, essv5884567, essv6304481, essv6488816, essv5823864, essv5664340, essv5613852, essv6190007, essv5447348, essv5495786, essv6312744, essv6234254, essv6390344, essv5933220, essv6489260, essv6102833, essv6152113, essv5494745, essv5573405, essv5916997, essv6472954, essv5843094, essv5886952, essv6425031, essv5620881, essv6157949, essv6529824, essv5789885, essv6364034, essv5519070, essv5738050, essv6075615, essv5641512, essv5677850, essv5495970, essv6530184, essv5899627, essv6298627, essv6291595, essv6271712, essv5712654, essv6385950, essv5442079, essv6347797, essv6246443, essv5877650, essv6007880, essv5523601, essv5631095, essv6519355, essv5887026, essv6370352
SamplesHG01060, HG00524, HG01052, HG01374, HG00315, NA18606, NA19920, HG00693, HG00337, HG00327, HG00271, NA19076, HG01350, HG01366, HG00501, HG01351, HG00689, HG00330, HG01492, HG01354, HG01365, HG00334, HG00537, HG00158, HG00281, HG01067, HG01170, HG00236, HG00325, HG00427, NA18557, HG01048, NA18985, HG00326, HG00464, HG00108, HG01353, HG00313, HG00133, HG01136, NA19657, HG01171, HG00701, NA19455, NA19663, HG00436, HG00275, NA18534, HG00619, NA19776, HG00708, HG00324, HG01073, HG00331, HG00684, HG00613, HG00140, HG01334, HG00276, HG00463, HG00258, NA18542, HG00285, NA19834, NA18543, HG00375, HG00278, HG01174, HG01375, HG00607, NA19679, HG01108, HG00620, HG00339, HG00125, NA19818, HG00259, HG00329, HG00342, NA18636, HG00310, HG00186, HG00280, HG00252, HG01125, HG01061
Known GenesB9D2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659362
Frequency
Sample Size1151
Observed Gain0
Observed Loss86
Observed Complex0
Frequencyn/a


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