A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621844



Internal ID6662020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129764130..129768243hg38UCSC Ensembl
Innerchr9:129764130..129768243hg38UCSC Ensembl
Outerchr9:129763828..129768578hg38UCSC Ensembl
chr9:132526409..132530522hg19UCSC Ensembl
Innerchr9:132526409..132530522hg19UCSC Ensembl
Outerchr9:132526107..132530857hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384114
hg194114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13628822, essv13628781, essv13628784, essv13628803, essv13628826, essv13628801, essv13628818, essv13628773, essv13628771, essv13628796, essv13628776, essv13628802, essv13628812, essv13628767, essv13628809, essv13628795, essv13628768, essv13628774, essv13628824, essv13628820, essv13628823, essv13628817, essv13628813, essv13628782, essv13628793, essv13628797, essv13628772, essv13628810, essv13628798, essv13628808, essv13628786, essv13628821, essv13628779, essv13628783, essv13628770, essv13628789, essv13628787, essv13628807, essv13628811, essv13628775, essv13628777, essv13628806, essv13628794, essv13628785, essv13628788, essv13628815, essv13628780, essv13628814, essv13628804, essv13628819, essv13628816, essv13628792, essv13628769, essv13628799, essv13628778, essv13628805, essv13628791, essv13628825, essv13628790, essv13628800
SamplesHG01303, NA19466, NA19020, HG02323, NA20298, HG03139, HG03172, NA19374, NA19201, NA19315, HG02952, NA19119, HG02854, NA19023, NA19138, HG03189, HG02471, NA20412, HG03380, HG02502, HG02946, NA20342, HG03058, NA18908, HG02477, HG02479, HG02716, HG03343, NA19327, HG01882, NA18915, NA18910, HG03294, HG03311, HG03085, HG02429, HG03388, NA19338, HG02585, NA19035, NA19017, NA19308, NA19309, NA19834, NA19108, NA19712, HG02308, HG01205, HG02317, HG01108, HG03112, HG03157, NA19438, HG02646, HG03063, HG01914, NA18505, NA19129, NA19346, NA19214
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621844
Frequency
Sample Size2504
Observed Gain0
Observed Loss60
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer