Variant Details

Variant: esv3646299

Internal ID

7033044

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr20:62992183..62993889	hg38	UCSC Ensembl
Inner	chr20:62992184..62993888	hg38	UCSC Ensembl
Outer	chr20:62992182..62993890	hg38	UCSC Ensembl
	chr20:61623535..61625241	hg19	UCSC Ensembl
Inner	chr20:61623536..61625240	hg19	UCSC Ensembl
Outer	chr20:61623534..61625242	hg19	UCSC Ensembl

Cytoband

20q13.33

Allele length

Assembly	Allele length
hg38	1707
hg19	1707

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv16222383, essv16222291, essv16222363, essv16222367, essv16222273, essv16222309, essv16222323, essv16222360, essv16222366, essv16222286, essv16222337, essv16222333, essv16222310, essv16222372, essv16222374, essv16222382, essv16222353, essv16222306, essv16222312, essv16222282, essv16222352, essv16222336, essv16222297, essv16222288, essv16222275, essv16222335, essv16222305, essv16222362, essv16222364, essv16222341, essv16222387, essv16222330, essv16222320, essv16222315, essv16222274, essv16222324, essv16222356, essv16222277, essv16222334, essv16222300, essv16222349, essv16222376, essv16222389, essv16222316, essv16222388, essv16222385, essv16222369, essv16222345, essv16222302, essv16222365, essv16222354, essv16222287, essv16222359, essv16222303, essv16222304, essv16222346, essv16222281, essv16222321, essv16222373, essv16222327, essv16222296, essv16222278, essv16222301, essv16222378, essv16222326, essv16222331, essv16222295, essv16222377, essv16222329, essv16222355, essv16222386, essv16222380, essv16222294, essv16222283, essv16222384, essv16222347, essv16222332, essv16222325, essv16222348, essv16222313, essv16222358, essv16222370, essv16222284, essv16222285, essv16222314, essv16222381, essv16222328, essv16222379, essv16222351, essv16222343, essv16222292, essv16222317, essv16222339, essv16222279, essv16222390, essv16222350, essv16222322, essv16222368, essv16222318, essv16222338, essv16222319, essv16222361, essv16222308, essv16222342, essv16222311, essv16222293, essv16222289, essv16222375, essv16222307, essv16222276, essv16222298, essv16222371, essv16222290, essv16222280, essv16222357, essv16222340, essv16222344, essv16222299

Samples

NA19141, HG00142, HG03052, HG02433, HG02798, HG02891, NA18486, HG02323, NA18504, HG03295, HG03139, NA19920, HG03095, HG03837, HG03572, HG03436, NA20796, NA18519, HG02811, HG03765, HG03246, HG03105, HG03224, NA19384, HG02981, NA11930, NA19923, HG02143, NA12275, HG03520, HG02315, HG01495, HG03624, NA19036, NA18520, HG01133, HG03073, HG03055, HG02780, HG03270, HG00739, HG01524, NA21106, HG02009, HG03343, HG02943, HG02442, HG03780, HG02977, HG02570, NA19908, HG01248, HG02678, NA19043, NA19236, HG02887, NA20519, NA18910, HG03311, HG03382, HG03476, HG01536, HG02494, NA19042, NA11840, HG03388, NA20538, HG04155, NA19113, HG00140, HG03571, NA20282, HG03391, NA19225, NA18523, HG02586, HG02896, HG02594, HG02568, NA20534, HG02484, NA20296, HG02813, NA20851, HG03028, HG00155, HG02759, HG03367, NA20870, NA19435, HG03458, HG02611, NA20790, HG03469, HG03433, NA19324, HG02580, NA20281, HG03557, HG01489, NA20357, HG03112, HG02646, HG03279, HG01055, NA19093, HG01631, NA19116, HG03538, HG03445, HG02855, HG01111, NA19463, NA18522, HG03439, HG01583, HG00553, HG03196

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3646299

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	118
Observed Complex	0
Frequency	n/a