Variant Details

Variant: esv2664540

Internal ID

9930645

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr2:166591491..166591494	hg38	UCSC Ensembl
Outer	chr2:166591337..166591644	hg38	UCSC Ensembl
Inner	chr2:167448004..167448001	hg19	UCSC Ensembl
Outer	chr2:167447847..167448154	hg19	UCSC Ensembl

Cytoband

2q24.3

Allele length

Assembly	Allele length
hg38	308
hg19	308

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5898669, essv5525882, essv5744210, essv5849499, essv5505202, essv5565048, essv5959639, essv6126765, essv5755963, essv5422404, essv5434066, essv6557254, essv6292544, essv5506913, essv5889872, essv6036588, essv6298455, essv5772680, essv5742919, essv5759122, essv5862992, essv6149499, essv6111834, essv5822241, essv5974766, essv5730056, essv5441785, essv5891002, essv5671774, essv6039720, essv6088344, essv5920328, essv5868668, essv5574838, essv6145712, essv6580564, essv5665200, essv6414732, essv6059725, essv6588984, essv6467892, essv6271647, essv6242879, essv6133470, essv6226755, essv6349157, essv6144194, essv6451309, essv6015468, essv6518181, essv5609168, essv5997245, essv5989292, essv6537750, essv6278967, essv6414905, essv5984001, essv5911623, essv6051947, essv6389397, essv5411430, essv6229870, essv5736705, essv5479447, essv6444573, essv6036293, essv5953969, essv5568711, essv5499836, essv6598306, essv6172710, essv5631887, essv5593124, essv5818301, essv5543943, essv5569417, essv6208472, essv6367988, essv6208459, essv5634061, essv6095035, essv5683260, essv6377076, essv5984724, essv6336462, essv6322599, essv5751137, essv5735459, essv6464728, essv6339873, essv5646152, essv5659147, essv6363069, essv5606308, essv6056839, essv5649370, essv6499577, essv6513193, essv6169003, essv5882512, essv5792916, essv6396615, essv6478989, essv5896044, essv6029004, essv5751703, essv5535564, essv6535501, essv5618755, essv6062488, essv6508726, essv5475828, essv5433353, essv6558095, essv6188435, essv5868498, essv6155392, essv5466903, essv6059714, essv5809321, essv5502146, essv6569454, essv5560970, essv6004697, essv5829486, essv6103873, essv6201326, essv5982189, essv6388414, essv5611902, essv6369772, essv6396752, essv5515493, essv6562934, essv5518477, essv6055947, essv5474352, essv6298715, essv6565743, essv6055322, essv5677156, essv6577407, essv6206111, essv6188107, essv5979349, essv5488827, essv6493792, essv6584967, essv6510139, essv5739793, essv6009038, essv5779081, essv5672769, essv5884070, essv5916177, essv5731913, essv5448095, essv5448151

Samples

HG01060, HG00650, NA12717, HG01173, HG01356, NA19397, HG00249, NA11995, NA18861, NA10851, HG00524, NA19399, HG01052, HG00187, HG00257, HG01066, HG00318, NA19359, NA12751, NA18545, HG01456, NA19377, HG00449, NA20517, NA20507, HG00261, NA12750, HG00693, HG00327, HG00663, HG00138, HG01350, NA19379, HG01366, HG00251, HG01351, HG00702, NA18558, HG00330, NA18547, HG01492, NA18916, NA11918, HG00346, NA18571, HG01083, HG00334, HG00185, HG00537, NA19404, NA12761, HG00512, HG00281, NA12282, HG00277, HG01069, HG01080, HG01067, NA19383, HG00335, NA19372, NA19371, HG00422, HG01440, HG00309, HG00338, HG01133, HG00326, HG00323, NA11993, HG00464, HG00108, HG01124, HG01353, HG00543, HG00313, HG00137, HG00154, HG01187, HG01171, HG01384, NA19403, HG00328, NA12003, HG00657, NA19391, HG00436, HG00556, HG00320, HG00584, HG00583, HG00500, HG00275, NA18534, HG01390, HG01047, HG00324, HG00284, HG01073, NA18573, HG00273, HG00651, HG00250, HG00373, HG00331, NA12249, HG01383, NA18532, HG00321, NA12827, HG01334, HG00276, NA19225, NA18523, HG01107, NA18546, NA18542, NA12716, HG00254, NA19390, HG00336, HG00285, NA19147, HG00353, NA19072, HG00375, NA19732, HG01357, HG01494, HG00607, HG00237, NA19428, HG00319, HG01108, NA19360, HG00256, HG00339, HG00513, HG00656, NA19093, NA18609, HG00310, HG00280, HG00343, HG00274, HG00252, HG01377, HG00472, HG01125, NA18624, NA07000, NA18522, NA12154, NA18612, NA18549, HG01437, HG00581, NA18577

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2664540

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	158
Observed Complex	0
Frequency	n/a