A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599055



Internal ID6986103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189506683..189507596hg38UCSC Ensembl
Innerchr3:189506683..189507596hg38UCSC Ensembl
Outerchr3:189506390..189507907hg38UCSC Ensembl
chr3:189224472..189225385hg19UCSC Ensembl
Innerchr3:189224472..189225385hg19UCSC Ensembl
Outerchr3:189224179..189225696hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11266359, essv11266353, essv11266339, essv11266395, essv11266355, essv11266364, essv11266352, essv11266405, essv11266413, essv11266369, essv11266424, essv11266427, essv11266412, essv11266409, essv11266391, essv11266356, essv11266361, essv11266338, essv11266337, essv11266358, essv11266362, essv11266343, essv11266370, essv11266354, essv11266400, essv11266422, essv11266416, essv11266392, essv11266411, essv11266425, essv11266380, essv11266341, essv11266408, essv11266433, essv11266418, essv11266410, essv11266342, essv11266378, essv11266423, essv11266345, essv11266371, essv11266366, essv11266421, essv11266404, essv11266346, essv11266414, essv11266393, essv11266375, essv11266372, essv11266429, essv11266379, essv11266384, essv11266385, essv11266348, essv11266387, essv11266428, essv11266417, essv11266430, essv11266431, essv11266383, essv11266396, essv11266390, essv11266386, essv11266398, essv11266403, essv11266402, essv11266399, essv11266347, essv11266340, essv11266368, essv11266360, essv11266401, essv11266367, essv11266389, essv11266374, essv11266365, essv11266381, essv11266394, essv11266397, essv11266406, essv11266419, essv11266357, essv11266432, essv11266388, essv11266415, essv11266377, essv11266344, essv11266349, essv11266373, essv11266407, essv11266420, essv11266350, essv11266426, essv11266376, essv11266351, essv11266363, essv11266382
SamplesHG01521, NA20853, HG01054, NA18924, NA12286, HG03965, NA20508, NA18861, NA19914, NA20783, HG01537, HG02648, HG03738, HG02318, NA12340, NA20507, NA20863, NA18510, NA20806, HG01694, HG01140, HG04059, NA20861, NA20890, NA20774, HG03736, HG03905, HG03978, HG03911, HG00243, HG02111, HG01893, HG02493, HG02490, NA20775, HG03788, HG01626, HG03114, NA12748, HG00108, HG01603, NA10847, HG02442, HG03908, HG01501, HG02322, HG03711, HG02450, NA20862, HG03900, HG01607, HG01615, HG01512, HG03824, HG01197, NA19031, HG02657, NA19750, HG01791, HG03625, HG04189, HG01101, HG03672, HG01708, HG01988, HG01075, NA20821, HG03238, HG03809, HG00336, HG02501, HG02790, HG00638, NA20804, HG01620, NA19741, HG04090, HG03108, HG03703, HG00107, NA19248, HG03066, HG02230, HG02235, NA19468, NA21101, NA21093, HG04098, NA19780, NA19030, HG01111, HG01125, NA12890, HG03118, NA20754, HG03196, HG01608
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599055
Frequency
Sample Size2504
Observed Gain0
Observed Loss97
Observed Complex0
Frequencyn/a


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