Variant Details

Variant: esv3597710

Internal ID

6984848

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr3:128595415..128596224	hg38	UCSC Ensembl
Inner	chr3:128595418..128596221	hg38	UCSC Ensembl
Outer	chr3:128595412..128596227	hg38	UCSC Ensembl
	chr3:128314258..128315067	hg19	UCSC Ensembl
Inner	chr3:128314261..128315064	hg19	UCSC Ensembl
Outer	chr3:128314255..128315070	hg19	UCSC Ensembl

Cytoband

3q21.3

Allele length

Assembly	Allele length
hg38	810
hg19	810

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv11138302, essv11138376, essv11138314, essv11138343, essv11138377, essv11138298, essv11138358, essv11138327, essv11138292, essv11138294, essv11138344, essv11138317, essv11138346, essv11138362, essv11138348, essv11138331, essv11138300, essv11138334, essv11138284, essv11138370, essv11138324, essv11138371, essv11138311, essv11138304, essv11138275, essv11138357, essv11138308, essv11138316, essv11138354, essv11138363, essv11138296, essv11138340, essv11138365, essv11138360, essv11138310, essv11138366, essv11138333, essv11138367, essv11138281, essv11138361, essv11138318, essv11138369, essv11138295, essv11138312, essv11138352, essv11138286, essv11138328, essv11138337, essv11138350, essv11138315, essv11138323, essv11138306, essv11138364, essv11138307, essv11138338, essv11138353, essv11138326, essv11138313, essv11138291, essv11138378, essv11138274, essv11138289, essv11138319, essv11138341, essv11138359, essv11138375, essv11138372, essv11138280, essv11138288, essv11138345, essv11138303, essv11138309, essv11138278, essv11138320, essv11138321, essv11138329, essv11138355, essv11138368, essv11138347, essv11138322, essv11138301, essv11138293, essv11138342, essv11138374, essv11138330, essv11138285, essv11138325, essv11138373, essv11138299, essv11138339, essv11138277, essv11138282, essv11138283, essv11138290, essv11138351, essv11138335, essv11138336, essv11138332, essv11138297, essv11138356, essv11138287, essv11138276, essv11138305, essv11138349, essv11138279

Samples

HG01986, NA19028, HG01054, NA19397, NA18924, HG03052, HG03175, NA19378, HG02433, HG02337, HG03300, HG03241, HG02419, NA19350, NA19092, HG03280, NA20294, HG03455, NA19393, HG03100, HG03295, HG00737, HG02536, NA19920, NA20359, HG03199, HG03572, HG03385, NA19315, HG03499, NA19307, NA19198, HG03370, HG02860, HG03479, HG01668, NA19384, HG02816, HG03209, NA19041, NA19383, NA18874, HG03212, NA19317, NA19026, HG03225, NA19239, NA19445, NA19025, HG03583, HG02879, HG02009, HG03343, NA18934, NA19403, NA19152, NA19043, HG01088, NA18910, HG02508, HG03085, NA19114, NA19118, NA19042, HG03446, HG03571, NA20282, HG02979, HG01890, HG02635, NA18858, HG01990, NA19401, NA19147, HG02308, NA19435, NA19331, HG01958, NA19380, NA20362, HG02941, NA19324, NA19310, HG02464, HG03557, HG02771, NA19376, NA19117, NA19472, HG03097, HG03066, HG02235, NA19474, HG03063, HG02768, HG02013, HG02861, NA19146, NA18488, HG01082, HG03376, HG02805, HG02284, HG03129, NA19431

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3597710

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	105
Observed Complex	0
Frequency	n/a