A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644439



Internal ID7031194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43035486..43091727hg38UCSC Ensembl
Innerchr19:43035986..43091227hg38UCSC Ensembl
Outerchr19:43034486..43092727hg38UCSC Ensembl
chr19:43539638..43595879hg19UCSC Ensembl
Innerchr19:43540138..43595379hg19UCSC Ensembl
Outerchr19:43538638..43596879hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3856242
hg1956242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv663e214
Supporting Variantsessv16058831, essv16058803, essv16058843, essv16058807, essv16058824, essv16058813, essv16058844, essv16058838, essv16058797, essv16058832, essv16058845, essv16058801, essv16058815, essv16058817, essv16058821, essv16058822, essv16058820, essv16058836, essv16058841, essv16058854, essv16058790, essv16058804, essv16058818, essv16058819, essv16058816, essv16058834, essv16058814, essv16058800, essv16058856, essv16058795, essv16058857, essv16058842, essv16058846, essv16058794, essv16058830, essv16058851, essv16058847, essv16058848, essv16058799, essv16058853, essv16058823, essv16058850, essv16058806, essv16058839, essv16058827, essv16058812, essv16058808, essv16058791, essv16058796, essv16058829, essv16058852, essv16058798, essv16058825, essv16058861, essv16058837, essv16058859, essv16058849, essv16058805, essv16058833, essv16058835, essv16058789, essv16058826, essv16058811, essv16058858, essv16058793, essv16058855, essv16058840, essv16058828, essv16058809, essv16058810, essv16058860, essv16058792, essv16058788, essv16058802
SamplesNA12842, NA19397, HG03163, NA20274, HG01815, HG03449, NA18999, HG02891, HG03455, NA12058, HG03792, NA20517, HG03069, NA12155, HG03074, HG01350, HG01325, HG02153, HG01366, NA20774, NA19916, HG03673, HG01354, NA18498, HG01110, HG03209, HG02143, HG02561, HG02315, NA18874, NA20775, HG02573, HG01519, HG02471, HG01048, HG03583, HG02409, HG04075, HG02479, HG00176, HG03547, HG01882, HG02554, HG02144, HG00320, HG03301, HG02429, NA18856, HG02649, NA19338, HG01936, NA19625, HG03064, NA19375, NA21113, NA18542, HG02667, NA19834, NA18543, NA19256, NA19147, NA20276, HG02941, HG01620, HG01798, NA19376, NA18501, HG02052, HG01883, HG01082, HG02284, NA18522, HG02406, HG00255
Known GenesPSG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644439
Frequency
Sample Size2504
Observed Gain0
Observed Loss74
Observed Complex0
Frequencyn/a


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