A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600357



Internal ID6987401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42704109..42707417hg38UCSC Ensembl
Innerchr4:42704109..42707417hg38UCSC Ensembl
Outerchr4:42703706..42707722hg38UCSC Ensembl
chr4:42706126..42709434hg19UCSC Ensembl
Innerchr4:42706126..42709434hg19UCSC Ensembl
Outerchr4:42705723..42709739hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383309
hg193309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11410834, essv11410804, essv11410801, essv11410775, essv11410853, essv11410791, essv11410835, essv11410820, essv11410825, essv11410842, essv11410803, essv11410833, essv11410832, essv11410818, essv11410811, essv11410851, essv11410808, essv11410772, essv11410816, essv11410785, essv11410784, essv11410840, essv11410770, essv11410830, essv11410837, essv11410831, essv11410847, essv11410839, essv11410850, essv11410777, essv11410805, essv11410794, essv11410767, essv11410817, essv11410797, essv11410821, essv11410795, essv11410854, essv11410822, essv11410768, essv11410845, essv11410807, essv11410849, essv11410779, essv11410838, essv11410852, essv11410798, essv11410824, essv11410782, essv11410827, essv11410776, essv11410848, essv11410761, essv11410841, essv11410814, essv11410765, essv11410812, essv11410796, essv11410826, essv11410844, essv11410828, essv11410760, essv11410778, essv11410836, essv11410846, essv11410815, essv11410786, essv11410774, essv11410783, essv11410829, essv11410762, essv11410787, essv11410810, essv11410800, essv11410780, essv11410781, essv11410813, essv11410809, essv11410771, essv11410759, essv11410819, essv11410799, essv11410789, essv11410792, essv11410758, essv11410788, essv11410793, essv11410769, essv11410773, essv11410806, essv11410766, essv11410790, essv11410802, essv11410823, essv11410764, essv11410843, essv11410763
SamplesHG03096, HG01412, NA19222, HG02628, HG01303, HG00102, NA11829, NA20531, NA18486, HG03280, NA12058, HG02888, NA19098, HG02895, NA12399, HG03572, NA20796, HG03168, HG02810, HG01702, NA19119, NA20317, HG03485, NA20769, HG03342, NA19197, HG03105, HG01063, HG03224, HG03793, HG02281, NA19922, HG00130, HG02703, HG02561, HG03556, HG03045, NA19456, NA19445, HG03583, NA20318, NA19027, HG03160, HG00380, HG00282, NA19403, HG01669, NA12003, NA20536, HG02253, HG04162, HG02470, HG01094, HG03563, NA18856, HG02649, HG02884, HG01182, HG03451, HG03391, HG02979, HG03046, HG00276, HG01708, HG01990, HG01700, NA19035, HG03064, HG00254, HG00119, NA19321, HG03367, HG02501, HG00366, HG02314, NA19360, HG03557, HG02814, HG03108, NA20888, HG03039, HG03442, NA19438, HG01935, NA19779, HG02107, NA19093, HG01089, HG01631, HG00234, NA19780, HG02052, HG02861, HG02643, HG01191, NA19429, HG01976
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600357
Frequency
Sample Size2504
Observed Gain0
Observed Loss97
Observed Complex0
Frequencyn/a


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