A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673748



Internal ID9593167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110208158..110211064hg38UCSC Ensembl
Outerchr10:110207787..110211534hg38UCSC Ensembl
Innerchr10:111967916..111970822hg19UCSC Ensembl
Outerchr10:111967545..111971292hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg383748
hg193748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5871393, essv5981721, essv6366785, essv5459638, essv6479185, essv6343244, essv5710295, essv6325065, essv6475472, essv5605931, essv5518449, essv5405324, essv6242761, essv6031746, essv5729251, essv6002732, essv5635744, essv5645929, essv6410924, essv6523661, essv5531586, essv5823831, essv6068709, essv5726167, essv5440197, essv6187120, essv6256025, essv6058263, essv5448895, essv6126608, essv5792797, essv6389156, essv5571933, essv5772448, essv5700911, essv5882312, essv6546413, essv6389871, essv6425629, essv6091784, essv5873607, essv6544736, essv5552747, essv6430303, essv5416531, essv6023609, essv5724661, essv5575653, essv6398558, essv6418224, essv5537013, essv6082926, essv6222006, essv6302542, essv6096929, essv6030864, essv6469701, essv6100203, essv5889828, essv6257030, essv6234444, essv5457742, essv6115713, essv5996520, essv5940234, essv6272708, essv5580477, essv5665312, essv6367354, essv5839610, essv6206742, essv5806887, essv5970742, essv5615127, essv5611306, essv5548400, essv6557879, essv5457952, essv6380487, essv5598360, essv6287598, essv5764584, essv5733273, essv5479465, essv5657520, essv5755927, essv6281932, essv5792061, essv5817564, essv6332880, essv5415040, essv5908513, essv5942060, essv6575406, essv5971573, essv6526587, essv6311853, essv5573973, essv6013626, essv5983744, essv5724111, essv6192924, essv5690493, essv6511385, essv5850275
SamplesHG01060, HG00189, HG01173, HG01098, HG01052, HG01079, HG01188, HG00315, HG00318, HG00181, HG00737, HG00179, HG01051, HG00337, HG00327, HG00271, HG01070, HG00272, HG00173, HG01168, HG00736, HG00346, HG01083, HG00270, HG00334, HG00185, HG00311, HG00281, HG00277, HG01069, HG01067, HG00335, HG01170, HG00325, HG01072, HG00309, HG00182, HG01198, HG00338, HG01048, HG00326, HG00178, HG00313, HG01183, HG00268, HG00266, HG00183, HG00176, HG01187, HG01171, HG00282, HG00328, HG00190, HG00732, HG01095, HG00368, HG00320, HG00344, HG00275, HG01047, HG01102, HG00324, HG00284, HG01073, HG00273, HG00373, HG01197, HG00331, HG01182, HG01101, HG00321, HG00276, HG01107, HG01204, HG01075, HG01190, HG00336, HG00285, HG00366, HG00353, HG00375, HG00734, HG00278, HG01174, HG00319, HG01108, HG00339, HG00269, HG00312, HG00329, HG00342, HG00267, HG00310, HG00186, HG00280, HG00343, HG00377, HG00372, HG00274, HG01082, HG00345, HG01097, HG01191, HG00180, HG01061
Known GenesMXI1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673748
Frequency
Sample Size1151
Observed Gain0
Observed Loss105
Observed Complex0
Frequencyn/a


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