Variant Details

Variant: esv2664914

Internal ID

9931019

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr16:69820428..69824902	hg38	UCSC Ensembl
	chr16:69854331..69858805	hg19	UCSC Ensembl

Cytoband

16q22.1

Allele length

Assembly	Allele length
hg38	4475
hg19	4475

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv503e199

Supporting Variants

essv6393966, essv6065695, essv6347187, essv5403751, essv5624940, essv5592966, essv6117791, essv5962860, essv6567495, essv6145314, essv5734526, essv5453490, essv6299449, essv6295298, essv6444053, essv6294397, essv6074040, essv6194060, essv5550427, essv6420895, essv6527169, essv5649884, essv6008830, essv5414501, essv6434500, essv6447534, essv5910536, essv5645384, essv6005173, essv6563040, essv6523867, essv6309620, essv6072503, essv5715366, essv5985348, essv6132934, essv6168929, essv6336273, essv6364865, essv5826679, essv5414928, essv6407306, essv6087717, essv5659859, essv6178953, essv5396476, essv6286658, essv6343009, essv6592771, essv5942075, essv6324253, essv6181237, essv5883730, essv5843926, essv5909305, essv5579639, essv5852209, essv6541263, essv6342755, essv6392001, essv5563396, essv5957171, essv5749433, essv6111155, essv6234247, essv6452761, essv5584194, essv5847118, essv5646808, essv6495074, essv5505155, essv5936686, essv5438803, essv6220821, essv5745745, essv5589378, essv6113993, essv6040353, essv5909057, essv5722766, essv5423847, essv5414524, essv6301723, essv5783447, essv5620829, essv5619922, essv5796108, essv6548026, essv6272927, essv6174354, essv5823019, essv6590639, essv5899858, essv5726580, essv6258727, essv6405875, essv6377916, essv5807792, essv6462843, essv5748461, essv6318087, essv5925066, essv5699458, essv5623922, essv6508973, essv5755854, essv5991415, essv6523129, essv6183845, essv6222140, essv5927963, essv6036423, essv6141405, essv6064306, essv6472637, essv6341673, essv5464261, essv6099050, essv6155395, essv5568016, essv5924284, essv5881412, essv6266313, essv6198401, essv5503238, essv6399163, essv5810435, essv5724889, essv6447171, essv6309301, essv5437641, essv6351712, essv5750998, essv5641984, essv5477344, essv5474041, essv5566371, essv5529528, essv5669463, essv5562386, essv6352059, essv5728018, essv5489150, essv5841792, essv5505374, essv6306918, essv6009844, essv6515681, essv6097003, essv5907840, essv5828564, essv6219958, essv6576103, essv6100562, essv6232244, essv6219204, essv5714732, essv5624800, essv5502138, essv6174383, essv5852147, essv5643599, essv6364006, essv5799625, essv5616149, essv6370808, essv6012532, essv5945425, essv5443421, essv5419969, essv5672293, essv6377724, essv6358884, essv5873463, essv6516483, essv5498219, essv6567287, essv6538722, essv6433170, essv5847926, essv5810480, essv5679832, essv5903990, essv5597097, essv5662868, essv6529085, essv6406269, essv5519517, essv5666497, essv6591064, essv6195496, essv5946991, essv5589472, essv5542157, essv5469366, essv6531446, essv6471688, essv5947653, essv5631956, essv5924758, essv6381850, essv6031771, essv6362334, essv5479191, essv5942534, essv5710054, essv5871132, essv5755162, essv6108268, essv5907685, essv5858480, essv5567714, essv6343290, essv5794235, essv5586938, essv5572511, essv6019123, essv5908150

Samples

HG01060, HG01441, NA19648, HG01173, HG01521, HG00608, NA12286, NA11829, HG00671, HG00559, NA18561, NA11920, NA20813, HG00233, NA20802, NA12045, HG01465, NA20805, NA19777, NA19057, NA18959, NA20808, NA20346, HG01518, HG00150, HG01461, HG00654, NA12400, HG01051, NA20771, NA12399, NA20806, HG01522, HG01140, NA18988, NA12413, HG00327, NA20814, NA20537, NA07346, NA20796, HG00251, HG00501, HG00122, HG01351, HG01177, HG00702, NA20586, NA20774, HG01168, NA20795, NA18547, HG01492, HG00736, NA19649, NA19062, NA20768, HG00334, NA19782, NA19681, HG00185, NA20336, NA18964, HG00311, NA20541, HG01134, NA20539, NA12282, NA12275, NA12005, HG01455, HG01069, HG01080, HG00120, HG00106, HG01519, HG00236, NA18977, NA20340, HG00422, HG00705, NA18986, NA19087, NA12889, HG00160, HG00159, NA18557, HG01133, NA20342, HG00178, NA20757, NA18973, HG01550, NA20515, NA19789, NA18539, HG00739, NA20753, HG01124, NA19007, NA10847, HG00313, HG00137, HG00133, NA12777, HG00188, HG00149, NA18951, NA18544, NA19247, NA18613, HG00629, NA19657, HG00266, HG01187, NA19070, NA19056, NA20787, NA19670, NA12342, NA20505, NA19077, NA12003, HG01515, NA18991, NA19663, HG00533, NA19788, NA18948, NA18534, NA20770, HG00619, NA18907, NA18537, NA19654, HG01102, HG01073, HG00651, NA19000, NA19084, NA19655, HG00404, HG00373, HG00479, NA11893, HG01197, NA12249, HG00117, HG01101, HG00613, NA18555, NA19318, NA12778, HG00246, NA18634, NA12546, NA19675, NA18541, HG01204, NA18576, HG00124, NA19652, HG00254, NA18952, NA20276, NA12775, HG00366, NA19473, NA12272, HG01253, HG00734, HG00638, NA07051, HG01174, NA20792, HG00237, NA19679, NA19786, HG00116, NA20516, NA20803, NA07037, NA19783, NA12763, NA06986, NA19398, HG00672, HG00513, HG01491, NA20582, NA19779, HG00329, HG00656, HG00342, NA20334, HG00267, NA12830, NA20786, NA11843, NA20758, NA20826, NA18552, NA18983, HG00377, HG00372, NA19661, HG00472, NA11892, NA19004, HG01082, HG01125, NA12890, NA07000, NA20585, NA12154, HG01097, HG00554, NA20772

Known Genes

WWP2

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2664914

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	218
Observed Complex	0
Frequency	n/a