A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656745



Internal ID9922850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37418837..37422429hg38UCSC Ensembl
chr17:35778921..35782535hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383593
hg193615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv550e199
Supporting Variantsessv6569824, essv6220771, essv6572972, essv5910829, essv5744333, essv5637134, essv6460897, essv6253626, essv6051006, essv6558244, essv5997487, essv6290050, essv6328991, essv6075994, essv5599204, essv5581662, essv6426152, essv6039636, essv5841219, essv6188471, essv6421431, essv6071246, essv6461919, essv5747548, essv5863394, essv6419411, essv5565766, essv5980898, essv6346508, essv6317760, essv5469686, essv5403151, essv5954529, essv5422731, essv6486956, essv5828130, essv5993586, essv6237584, essv6524080, essv6042427, essv6258061, essv6375147, essv5637933, essv5770574, essv5755605, essv5882150, essv6566854, essv6503739, essv6367648, essv6195154, essv5686072, essv5852949, essv6471070, essv5611549, essv6218498, essv6039138, essv6243154, essv6111864, essv5687998, essv6554815, essv6363163, essv5622135, essv5573254, essv6155219, essv5642510, essv6541492, essv6434727, essv6524380, essv6158281, essv5950276, essv5901770, essv6232730, essv5401971, essv6288983, essv5464999, essv6560754, essv6084238, essv5403740, essv6397485, essv6093480, essv6393570, essv6349923, essv5540617, essv6507661, essv5773340, essv6205919, essv5675337, essv5663322, essv5532948, essv5510570, essv6314202, essv5594663, essv5459250, essv5511967, essv6455883, essv6183368, essv5413534, essv6106812, essv6008883, essv5786914, essv6099661, essv6429527, essv6156418, essv6295650, essv6496311, essv6113019, essv6493152, essv6335977, essv6081486, essv5594873, essv6386257, essv6245930, essv5687294, essv6064684, essv5533641, essv6288961, essv6282361, essv5825228, essv5738427, essv5727730, essv5973218, essv5727165, essv5976198, essv6272317, essv5905424, essv5490299, essv6553495, essv6479733, essv6180808, essv5853370, essv5550605, essv6540237, essv5951250, essv6590718, essv6119221, essv6577577, essv6102771, essv6263931, essv5991296, essv5950422, essv5455621, essv6036278, essv6118554, essv6369227, essv6130101, essv5567499, essv6190329, essv5885445, essv5851716, essv5780797, essv5847628, essv5591667, essv6081555, essv5692048, essv5651964, essv5678793, essv6170041, essv6349519, essv6277442, essv5642472, essv6169412, essv5922382, essv5434689, essv6434052, essv5775800, essv5862668, essv6105499, essv5833945, essv5746931, essv6373611, essv6447356, essv6282226, essv6110470, essv5814031, essv6386453, essv6142699, essv5688993, essv6449292, essv6125460, essv5974193, essv6581383, essv6239167, essv5549965, essv5994567, essv5686166, essv5931037, essv6582696, essv5672122, essv6148514, essv6296485, essv6523773, essv5517397, essv6440354, essv5512475, essv6460784, essv5672600, essv6032865, essv6036959
SamplesNA19312, NA19063, NA19065, HG00554, HG01191, NA19074, HG00553, HG00581, NA18577, NA18620, HG00626, HG01060, HG00189, HG00114, NA20761, HG00650, NA19648, NA11830, HG01173, NA19058, NA20529, HG01521, NA20543, NA18621, NA19066, NA18861, HG00559, NA20531, HG00315, HG00151, NA20752, NA20802, NA18603, HG00699, NA18596, NA18530, NA20808, NA18616, HG01518, NA20507, HG00654, NA18526, NA18633, NA12155, NA07357, HG01522, HG00663, NA07346, HG00138, HG01350, NA18944, HG00589, NA18597, NA18489, NA18595, HG00689, NA18982, NA18619, HG00330, HG00634, HG00610, NA19062, NA18574, HG01354, HG00247, NA19054, HG00334, NA20287, NA18964, HG00537, HG00590, NA20541, NA11930, HG01134, NA20759, HG01080, HG01067, HG00120, NA19383, NA06984, HG01170, HG00236, NA19719, HG00232, NA20340, NA12044, NA19075, NA18617, HG00422, HG01440, HG00309, NA19002, HG00118, NA18990, NA20533, NA18908, HG00323, HG00530, NA20515, NA20755, HG00464, HG00108, NA20818, NA18614, HG00313, HG00137, NA18544, NA19908, HG00183, NA19056, HG00596, NA12342, NA12003, NA20809, HG00577, NA20810, NA20760, NA20536, NA19391, HG00475, HG00556, HG00320, HG00583, NA18637, HG00500, HG00275, NA18579, NA18572, NA18534, HG00619, HG00239, NA20525, NA19654, HG01102, HG00651, NA19000, NA18626, HG00690, HG00404, HG00373, HG00479, HG01197, HG00331, HG01383, HG00525, HG00321, HG00140, NA12827, NA19059, NA18536, NA18570, NA18634, NA12043, NA19401, NA19003, NA18632, NA20522, NA18542, NA18535, HG00285, HG00265, NA18961, NA18952, NA18564, NA18628, HG00580, HG00357, NA19773, NA07051, NA19010, NA12046, NA20544, HG00319, HG00116, NA20797, NA07037, HG00256, NA19783, HG01489, NA06986, NA19818, NA18501, HG00614, HG01491, HG00656, HG01055, HG00174, NA20510, HG00112, NA20758, HG00343, NA20528, NA19900, NA18983, NA20503, HG01377, HG00472, NA11892
Known GenesTADA2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656745
Frequency
Sample Size1151
Observed Gain0
Observed Loss198
Observed Complex0
Frequencyn/a


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