Variant Details

Variant: esv3647726

Internal ID

7034466

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr22:38340567..38341892	hg38	UCSC Ensembl
Inner	chr22:38340617..38341843	hg38	UCSC Ensembl
Outer	chr22:38340518..38341942	hg38	UCSC Ensembl
	chr22:38736572..38737897	hg19	UCSC Ensembl
Inner	chr22:38736622..38737848	hg19	UCSC Ensembl
Outer	chr22:38736523..38737947	hg19	UCSC Ensembl

Cytoband

22q13.1

Allele length

Assembly	Allele length
hg38	1326
hg19	1326

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv16421344, essv16421234, essv16421291, essv16421240, essv16421224, essv16421289, essv16421238, essv16421312, essv16421309, essv16421342, essv16421239, essv16421350, essv16421293, essv16421252, essv16421278, essv16421349, essv16421326, essv16421230, essv16421295, essv16421275, essv16421266, essv16421314, essv16421269, essv16421318, essv16421313, essv16421297, essv16421253, essv16421229, essv16421288, essv16421279, essv16421271, essv16421310, essv16421305, essv16421322, essv16421319, essv16421260, essv16421281, essv16421268, essv16421336, essv16421303, essv16421323, essv16421286, essv16421267, essv16421294, essv16421272, essv16421324, essv16421254, essv16421244, essv16421325, essv16421304, essv16421227, essv16421321, essv16421300, essv16421306, essv16421316, essv16421307, essv16421236, essv16421311, essv16421249, essv16421255, essv16421332, essv16421243, essv16421285, essv16421341, essv16421265, essv16421335, essv16421262, essv16421259, essv16421257, essv16421233, essv16421287, essv16421290, essv16421302, essv16421274, essv16421276, essv16421296, essv16421338, essv16421247, essv16421345, essv16421242, essv16421346, essv16421337, essv16421317, essv16421237, essv16421225, essv16421231, essv16421258, essv16421228, essv16421256, essv16421251, essv16421246, essv16421245, essv16421301, essv16421264, essv16421328, essv16421248, essv16421339, essv16421282, essv16421261, essv16421347, essv16421235, essv16421232, essv16421348, essv16421333, essv16421298, essv16421270, essv16421327, essv16421250, essv16421277, essv16421241, essv16421351, essv16421263, essv16421329, essv16421299, essv16421280, essv16421284, essv16421330, essv16421334, essv16421292, essv16421226, essv16421331, essv16421343, essv16421340, essv16421320, essv16421273, essv16421308, essv16421315, essv16421283

Samples

NA19394, HG02890, HG02496, NA19397, HG03378, HG02583, NA19204, HG03163, NA19914, NA19332, HG02433, HG03247, NA18881, HG02798, HG03558, HG02804, HG03521, HG03295, NA19377, HG03126, HG03515, HG03297, HG03139, HG03577, NA19443, HG02769, NA19107, NA19374, HG03086, HG02621, HG03385, HG03452, HG02952, HG02325, HG03370, NA19131, HG02860, NA19023, NA20291, HG02922, HG02111, HG01242, NA19038, NA19922, NA19137, NA20340, NA19238, NA19024, HG03195, HG03352, HG02571, NA20412, HG03380, HG03225, HG02477, HG02570, HG03054, NA19403, NA19462, NA18933, HG03547, HG01882, HG02322, NA18516, HG03575, HG03159, HG03081, HG02968, HG02497, HG02470, HG02537, HG03311, HG03078, HG03446, NA19338, HG03391, HG02979, HG03046, HG02585, HG01286, HG03354, NA19395, NA18858, HG01956, HG01107, HG02675, HG02484, NA19436, HG02613, NA19390, NA18909, HG02799, HG02501, HG02308, HG01915, NA19037, HG03458, NA19144, HG02611, NA18865, NA19428, HG03473, HG01108, HG03557, HG03084, HG02771, NA19323, HG03565, NA20348, NA19248, HG02974, HG03442, NA19438, HG01912, HG03313, NA19093, HG03063, HG03258, HG02462, HG03351, NA19711, HG03077, HG03470, HG01914, NA19030, HG03118, HG03303, HG03196

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3647726

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	128
Observed Complex	0
Frequency	n/a