Variant Details

Variant: esv2673456

Internal ID

9592875

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr2:216633093..216637199	hg38	UCSC Ensembl
Outer	chr2:216632622..216637569	hg38	UCSC Ensembl
Inner	chr2:217497816..217501922	hg19	UCSC Ensembl
Outer	chr2:217497345..217502292	hg19	UCSC Ensembl

Cytoband

2q35

Allele length

Assembly	Allele length
hg38	4948
hg19	4948

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6038155, essv6038662, essv6443340, essv6235812, essv6085681, essv5909398, essv5555351, essv5593726, essv5725443, essv6083292, essv5532657, essv5488096, essv6060444, essv6108036, essv6546002, essv6258981, essv5632679, essv6431226, essv5899395, essv5908816, essv5962912, essv5572656, essv5775278, essv5920451, essv5795507, essv5745535, essv5499090, essv6494982, essv5659187, essv6397525, essv5423733, essv6362058, essv5654545, essv6304599, essv6225896, essv6005402, essv5808252, essv5884058, essv6157469, essv5833553, essv5417887, essv5727663, essv5430222, essv6207060, essv5895653, essv6364892, essv5988703, essv6243550, essv6098548, essv5915844, essv5502355, essv6394795, essv6185866, essv6408452, essv6436531, essv5497805, essv5547709, essv6081306, essv6003705, essv5918453, essv6051891, essv6521390, essv6340336, essv5766441, essv6438721, essv6127310, essv5516241, essv5632217, essv6252150, essv6025202, essv6049239, essv5526352, essv6418903, essv5813309, essv5616655, essv6477312, essv6200107, essv6332130, essv5896014, essv6212488, essv6189980, essv5684209, essv5944024, essv6445401, essv5900351, essv6200228, essv6335659, essv5944836, essv5899298, essv5567031, essv5817634, essv6267372, essv6522926, essv5478993, essv6293155, essv6136458, essv6118988, essv6124847, essv5706584, essv6289648, essv6458800, essv5688171, essv6481018, essv6346668, essv5397966, essv5779280, essv5815513, essv6208585, essv5841740, essv6445491, essv5766231, essv5565740, essv6382284, essv6272692, essv6118384

Samples

HG00626, HG00403, HG00189, HG00542, HG00536, HG00608, HG00671, HG00361, HG00524, HG00315, HG00367, HG00318, HG00181, HG00699, HG00654, HG00693, HG00327, HG00271, HG00589, HG00272, HG00501, HG00448, HG00330, HG00634, HG00610, HG00346, HG00270, HG00334, HG00185, HG00537, HG00590, HG00512, HG00277, HG00335, HG00325, HG00534, HG00422, HG00705, HG00182, HG00427, HG00338, HG00178, HG00323, HG00530, HG00419, HG00313, HG00443, HG00268, HG00266, HG00176, HG00282, HG00596, HG00328, HG00428, HG00657, HG00368, HG00436, HG00320, HG00533, HG00583, HG00344, HG00500, HG00275, HG00619, HG00708, HG00635, HG00324, HG00284, HG00690, HG00404, HG00373, HG00531, HG00479, HG00331, HG00613, HG00525, HG00276, HG00704, HG00611, HG00476, HG00336, HG00285, HG00625, HG00353, HG00580, HG00375, HG00357, HG00278, HG00473, HG00607, HG00662, HG00418, HG00339, HG00269, HG00513, HG00578, HG00478, HG00421, HG00329, HG00656, HG00342, HG00174, HG00310, HG00186, HG00698, HG00280, HG00343, HG00372, HG00274, HG00595, HG00472, HG00628, HG00345, HG00437, HG00581

Known Genes

IGFBP2

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

High quality site

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2673456

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	115
Observed Complex	0
Frequency	n/a