A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658674



Internal ID9578093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36349849..36356170hg38UCSC Ensembl
chr19:36840751..36847072hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386322
hg196322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv638e199
Supporting Variantsessv6055392, essv5603918, essv6420361, essv6014279, essv6233140, essv6495802, essv6321638, essv5633587, essv6202451, essv6109465, essv6061404, essv5997446, essv6516112, essv6381354, essv6215425, essv5711015, essv5523031, essv5432270, essv6441963, essv6176369, essv5933557, essv5616097, essv6352032, essv5968456, essv5511816, essv6371684, essv5738076, essv5787031, essv5842505, essv5647919, essv6453360, essv6349027, essv6157586, essv5860893, essv5479950, essv6530074, essv5585007, essv6146223, essv5658670, essv5770348, essv5574395, essv5530385, essv5497680, essv6268291, essv5496838, essv5743736, essv5834859, essv6235592, essv5718402, essv6169523, essv5807376, essv6309152, essv6060944, essv6430141, essv6195738, essv5429346, essv6096634, essv6003227, essv6002093, essv5479252, essv6394200, essv6307933, essv6096623, essv5677213, essv6480230, essv6539888, essv5876038, essv5972815, essv5883884, essv5425138, essv6360912, essv5712778, essv6245183, essv6467141, essv6122859, essv6531518, essv5702782, essv6391203, essv6208007, essv5658538, essv6086124, essv5672598, essv6216145, essv6476703, essv6203907, essv5526011, essv5464209, essv6383452, essv5400650, essv6037857, essv5931687, essv5891179, essv6036557, essv6447768, essv5936506, essv5697603, essv5765911, essv5582597, essv6422880, essv6289511, essv5666689, essv6428066, essv6064745, essv5963198, essv5951257, essv6395865, essv6270095, essv6035864, essv6409403, essv6048449, essv5996929, essv6194828, essv6478623, essv6278388, essv6303163, essv5788796, essv5737655, essv6496728, essv5602065, essv6050668, essv6364720, essv5472140, essv6178852, essv6524821, essv5987524, essv6391332, essv5432657, essv5544524, essv6393964, essv6348565, essv5576605, essv5614342, essv6538837, essv6519768, essv5751815, essv6287841, essv6325439, essv6276596, essv6012612, essv6576377, essv6393300, essv6012306, essv5700842, essv6581618, essv6120450, essv5527762, essv6441746, essv5959924, essv6081134, essv6080030, essv6473268, essv6454414, essv6206990, essv5588853, essv5682122, essv6426506, essv5867402, essv5410764, essv6396353, essv6187619, essv5709986, essv6193436, essv6228421, essv5532774, essv6562484, essv5972388, essv5709267, essv5523522, essv5427525, essv6360612, essv5884526, essv5770770, essv5437839, essv5481874, essv6056368, essv5603243, essv5979101, essv6205047, essv6062357, essv5422720, essv6150271, essv6304558, essv6405365, essv6221304, essv6577177, essv6428231, essv5407121, essv5902863, essv5875211, essv5599539, essv5482898, essv6009818, essv5728896, essv6399034, essv6041351, essv6046592
SamplesHG01060, NA19700, NA19058, NA20529, HG01098, NA19055, HG00231, NA19909, HG00142, NA20766, NA18947, NA20508, NA18592, HG01052, NA18565, NA18561, HG01188, NA20532, HG00640, HG00181, NA20294, NA19777, HG00179, NA20346, HG00177, HG00150, NA18526, NA20771, NA20806, NA18602, HG00327, NA19068, HG00641, NA19746, HG00138, NA20796, NA20798, NA19762, NA19728, NA18595, HG01167, NA20586, NA20774, HG01168, NA18635, NA20756, NA18567, NA20317, NA19916, HG00330, HG00346, NA20540, NA19771, HG01083, HG00247, HG00334, NA19681, NA19904, NA18964, HG00243, HG00158, NA20541, NA20539, HG00277, HG01067, NA20278, HG00106, HG01170, NA18977, NA19917, HG00232, NA18560, NA18617, HG01176, NA19087, NA19901, HG01048, NA20533, NA19985, HG00253, NA18539, NA19921, HG00313, HG00154, HG00731, NA20800, HG00266, HG00176, HG01187, NA20524, HG00328, HG00732, NA19717, NA20314, NA19663, HG00344, NA19081, NA18637, NA19788, HG00275, NA20506, NA20519, NA18976, NA18630, NA19776, NA19064, HG01047, NA20525, NA19654, HG01073, NA18573, NA20299, HG00373, HG01182, HG01101, HG00140, NA20282, HG01334, NA19761, NA18555, HG00152, NA19682, NA20828, NA19756, HG00246, NA20542, HG01107, NA18541, NA18974, NA20765, NA20296, NA19003, HG00258, NA20799, HG00124, NA20522, NA20801, HG00254, HG00119, HG00285, NA18961, NA18543, NA18564, NA19749, HG00366, NA19732, HG00734, HG00638, NA20804, HG00278, NA20520, NA19010, HG01174, NA20790, NA20530, NA20778, HG00237, NA20504, NA20544, HG00319, NA19083, NA20797, NA19783, NA18615, NA18610, HG00339, HG00269, NA19759, NA19078, NA18971, NA19060, HG00329, NA18987, NA20334, NA19716, HG00267, NA19713, HG00123, HG00186, HG00131, NA20758, NA19080, NA19900, HG00252, NA20502, NA18984, NA18989, HG01082, NA18624, NA18623, NA19063, HG01097, HG00554, NA19074, NA18965, NA18577
Known GenesZFP14
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658674
Frequency
Sample Size1151
Observed Gain0
Observed Loss196
Observed Complex0
Frequencyn/a


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