Variant Details

Variant: esv2667868

Internal ID

9933973

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:152047141..152047581	hg38	UCSC Ensembl
	chr3:151764930..151765370	hg19	UCSC Ensembl

Cytoband

3q25.1

Allele length

Assembly	Allele length
hg38	441
hg19	441

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5629464, essv5584461, essv6587406, essv6123504, essv6553539, essv5482788, essv6287315, essv5677325, essv6018475, essv5433114, essv5928408, essv5911399, essv6265483, essv5984056, essv5740736, essv6255319, essv6104895, essv6453773, essv5713878, essv5679263, essv5678538, essv6300429, essv5952505, essv5833022, essv6111718, essv5730802, essv6502717, essv5911640, essv5593809, essv5443162, essv6577169, essv5451379, essv6259058, essv5429621, essv6352690, essv6009533, essv5809984, essv6183475, essv6005368, essv6223561, essv5498504, essv5647165, essv6555312, essv5532548, essv6144529, essv5606979, essv5989723, essv5963173, essv6048783, essv5508249, essv6371216, essv5852491, essv6477911, essv6315044, essv5413032, essv5985892, essv5654981, essv5993087, essv6053807, essv6008076, essv6575670, essv5917187, essv5983366, essv5947346, essv5956534, essv5651960, essv6130973, essv5410249, essv6319020, essv5601342, essv6207254, essv5778279, essv5610701, essv6282396, essv5446497, essv6565515, essv5722571, essv5823313, essv6427250, essv5680146, essv5599462, essv6056002, essv5798596, essv5734472, essv6264194, essv5485706, essv5582846, essv6329952, essv6221721, essv5617706, essv6536968, essv6310866, essv6507616, essv6442980, essv5713241, essv6037385, essv6536985, essv5965508, essv6516081, essv6178064, essv5991980, essv5459856, essv5967460, essv6544949, essv5423292, essv6189040, essv6074473, essv5418674, essv6239326, essv6273020, essv6473325, essv6396237, essv6383774, essv6097345, essv6500773, essv5555877, essv5901780

Samples

HG00403, NA19701, HG00442, NA19058, HG00592, NA19397, NA18947, HG00671, NA18861, HG01359, NA18980, NA18599, NA18603, NA19350, NA19819, NA18596, HG00566, NA18530, NA18616, NA18602, NA18988, NA18627, HG00327, HG00663, NA19396, NA19381, NA18550, HG00589, NA19382, NA19448, HG00702, HG00689, HG00448, NA18982, NA18635, NA18619, NA19916, NA19131, NA18618, HG00736, NA19904, NA19384, HG00311, NA19079, HG00590, HG01067, NA18868, NA18560, HG00422, HG00705, NA19159, HG00427, NA18985, NA18539, HG00464, HG00543, NA18951, NA18613, HG00443, NA18538, HG01360, HG01187, NA19070, NA19670, NA19403, HG00701, HG00475, NA18637, HG01498, HG00500, NA18548, NA18537, NA18566, HG00651, HG00479, NA18532, HG00321, NA19059, NA19009, HG00276, NA19225, NA18523, HG00463, NA18634, HG00611, HG00476, NA18543, NA18628, NA18950, HG01551, NA18941, NA19380, NA19428, NA19085, NA18610, NA19078, HG00478, NA18631, NA19060, NA18987, HG00656, NA19468, NA19093, NA18873, HG00698, NA19080, NA19213, NA18972, NA18983, NA18989, HG00628, NA18549, NA19074, HG00553, HG00437, NA18562, NA18965

Known Genes

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)

esv2667868

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	117
Observed Complex	0
Frequency	n/a