A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676825



Internal ID9596244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46464093..46464328hg38UCSC Ensembl
chr13:47038228..47038463hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6369538, essv5442654, essv5838693, essv5420279, essv5416903, essv6489189, essv6495496, essv5620784, essv6524570, essv5472147, essv5574483, essv6089516, essv6390767, essv6510965, essv6307987, essv6392544, essv5761460, essv5943112, essv5682921, essv5609833, essv6392729, essv5881898, essv6396216, essv5938815, essv5675069, essv6450664, essv6198901, essv6024828, essv6334143, essv5582181, essv5672283, essv6281042, essv6388957, essv5529992, essv5979151, essv6131105, essv6545961, essv5982137, essv6026634, essv5697206, essv5831643, essv5439357, essv6225373, essv6251580, essv6563831, essv5552922, essv6240969, essv5563261, essv5558524, essv6214893, essv6103488, essv5724884, essv5507497, essv5504080, essv5521956, essv5538908, essv6522465, essv5578133, essv5925029, essv6222020, essv5506987, essv6219429, essv5786822, essv6202290, essv5678173, essv5824755, essv5747448, essv6332758, essv5928649, essv6347907, essv6339561, essv5806383, essv5430023, essv5828192, essv5662488, essv5498296, essv5890886, essv5997039, essv5427243, essv5664899, essv6233449, essv5539833, essv5901825, essv5518950, essv5828739, essv5830033, essv6115878, essv6534574, essv5684861, essv5685783, essv5745632, essv5415246, essv6484153, essv6098712, essv6387446, essv5875868, essv6347156, essv5501736, essv6081443, essv5543448
SamplesHG01060, HG00143, HG00536, HG00249, HG01052, HG00257, HG01389, HG01066, HG00315, HG00318, NA18530, NA19443, HG00261, HG00693, HG00337, HG00327, HG01350, HG01351, HG00330, HG01492, HG00346, HG01083, HG01365, HG00334, HG00590, NA18611, HG00512, HG00277, HG01080, HG00335, HG01170, HG00236, HG00534, HG00422, HG00309, HG00338, HG01048, HG00323, HG00253, NA18638, HG00108, HG00543, HG00313, HG00137, HG00268, HG01187, HG01171, HG00282, HG00328, HG00320, NA18637, HG00263, HG00275, NA18534, HG00692, HG01390, HG01102, HG00324, HG00284, HG00684, HG01101, HG00613, HG00140, HG01334, HG00276, NA19225, HG00463, NA12546, NA18546, NA18542, HG00285, NA18543, HG00353, HG00375, HG00278, HG01174, HG01375, HG00607, HG01137, HG00319, HG01108, HG00256, HG00662, HG00339, HG00125, HG00672, HG00614, HG00111, HG00478, HG00329, HG01055, NA12830, HG00310, HG00274, HG00252, HG01082, NA18623, NA18549, HG01061, NA18577
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676825
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