A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2676825

Internal ID9596244
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46464093..46464328hg38UCSC Ensembl
chr13:47038228..47038463hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5504080, essv6524570, essv6563831, essv6219429, essv5875868, essv5662488, essv6387446, essv5415246, essv5979151, essv6369538, essv5684861, essv5682921, essv6098712, essv5724884, essv5675069, essv6545961, essv5563261, essv5430023, essv5838693, essv6522465, essv6214893, essv6281042, essv6489189, essv5427243, essv5574483, essv5582181, essv5938815, essv6339561, essv5747448, essv5890886, essv6081443, essv6307987, essv5685783, essv5498296, essv5442654, essv6131105, essv5830033, essv6334143, essv6534574, essv6396216, essv6510965, essv5416903, essv5664899, essv6251580, essv6024828, essv5786822, essv6222020, essv6347156, essv5558524, essv5672283, essv5420279, essv6202290, essv6392544, essv5539833, essv6388957, essv5521956, essv5745632, essv5578133, essv6450664, essv6390767, essv5761460, essv5828192, essv5901825, essv5925029, essv6103488, essv5543448, essv5997039, essv5472147, essv5943112, essv5552922, essv5506987, essv6332758, essv5831643, essv5678173, essv5620784, essv6225373, essv5609833, essv6240969, essv6392729, essv5501736, essv5518950, essv6026634, essv6198901, essv5824755, essv6115878, essv5928649, essv6347907, essv6089516, essv6495496, essv5697206, essv5529992, essv5538908, essv5507497, essv5806383, essv5828739, essv6233449, essv6484153, essv5439357, essv5881898, essv5982137
SamplesHG00323, HG00613, HG00309, HG00313, HG00252, HG00318, HG00536, HG00607, HG00257, NA18534, NA18530, HG01052, HG00328, HG01055, HG01083, HG00274, HG00310, HG00261, HG01389, HG00463, HG00614, HG01365, HG01492, HG01082, HG00375, HG01174, NA18542, HG01350, NA18546, HG00111, HG00334, HG00335, HG01101, HG00319, HG00253, HG01171, HG00353, HG00256, HG00543, HG00339, HG00346, HG01375, HG00337, HG00140, NA19443, NA18623, HG01048, HG01061, HG00692, HG00315, HG00330, NA18638, HG00338, HG00125, NA18637, HG00276, HG00284, HG01187, NA12830, HG00662, HG00108, HG00268, HG01066, HG00263, HG00672, HG00282, HG01170, HG00249, HG00478, HG00277, HG01080, HG01351, HG00329, HG00512, HG00534, HG01060, HG00236, NA18543, HG01137, HG00590, HG01334, NA18577, HG01390, HG00285, NA19225, NA12546, HG00422, HG01108, HG00693, NA18611, HG00320, HG00275, HG00324, NA18549, HG00137, HG01102, HG00684, HG00143, HG00278, HG00327
Known Genes
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2676825
Sample Size1151
Observed Gain0
Observed Loss100
Observed Complex0

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