Variant Details

Variant: esv2658820

Internal ID

9924925

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr16:4017047..4017527	hg38	UCSC Ensembl
	chr16:4067048..4067528	hg19	UCSC Ensembl

Cytoband

16p13.3

Allele length

Assembly	Allele length
hg38	481
hg19	481

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5633382, essv5940571, essv5525257, essv5484417, essv6355251, essv6535006, essv6488124, essv6121585, essv5770866, essv6525343, essv6516242, essv5591624, essv5699314, essv6358137, essv6244271, essv6193122, essv6418463, essv5935322, essv5882581, essv5905783, essv6377685, essv5838130, essv5688011, essv5476926, essv5729473, essv5674427, essv6475489, essv6048208, essv5545341, essv6427116, essv6059495, essv6314091, essv5981635, essv5493901, essv6407619, essv6026306, essv6463179, essv5989467, essv5546388, essv6206499, essv6450830, essv5440549, essv5607384, essv5671130, essv5629511, essv5478581, essv6556102, essv5434619, essv6578927, essv6171333, essv5940728, essv5872753, essv6586283, essv6228207, essv5886578, essv6410226, essv6190597, essv6200522, essv6326663, essv6563611, essv6091484, essv5541627, essv6597084, essv6334381, essv5819932, essv5662204, essv5427539, essv5944453, essv5415306, essv5507838, essv5396595, essv6443573, essv6387143, essv6055271, essv6221406, essv6259493, essv5995893, essv6369310, essv6033747, essv5667943, essv5474139, essv6273333, essv6381370, essv6595003, essv5569474, essv6016355, essv6556549, essv5846273, essv6071771, essv6131435, essv6159443, essv5830720, essv5657989, essv6159424, essv6374161, essv6114121, essv5753643, essv5426010, essv5774035, essv6310138, essv6052555, essv5963771, essv6589660, essv6260908, essv6500577, essv6479547, essv6082802, essv6052583, essv5701660, essv5770478

Samples

HG00536, HG00231, NA19664, HG00524, NA19914, HG00187, NA18565, HG01079, HG00100, HG01188, NA11931, NA18599, HG01374, NA20512, NA18603, HG00699, NA12004, HG01456, HG00566, NA18530, NA20808, HG00150, NA18526, NA18988, HG00271, NA18563, HG00641, NA19746, NA19076, HG01350, HG01070, NA19762, NA19728, HG01351, NA19678, NA19723, NA18982, HG01492, NA18582, NA18571, NA19054, NA19782, NA19079, HG00590, HG00158, HG01134, NA19720, NA19651, NA06984, NA19719, NA19238, NA12044, NA19731, NA18617, NA19722, NA19725, NA18990, NA18973, NA19789, NA18638, HG01124, NA19007, HG01136, HG00188, NA19657, NA19077, NA19152, NA20314, NA19663, HG00556, NA19788, NA18572, NA18948, NA18534, HG00740, NA19654, NA19114, NA18626, HG00531, HG00321, NA18555, NA19756, NA19675, HG01148, NA19729, NA19749, NA19072, NA19732, NA20520, NA19010, HG01375, HG01137, NA18943, NA19783, NA18610, NA19759, HG00672, NA19785, HG00267, HG00310, NA19726, NA19780, HG00343, NA18552, NA18983, HG00595, NA19758, NA18622, HG00553, HG00437

Known Genes

ADCY9

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2658820

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	110
Observed Complex	0
Frequency	n/a