A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601036



Internal ID6988075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75821760..75825008hg38UCSC Ensembl
Innerchr4:75821760..75825008hg38UCSC Ensembl
Outerchr4:75821260..75825508hg38UCSC Ensembl
chr4:76742913..76746161hg19UCSC Ensembl
Innerchr4:76742913..76746161hg19UCSC Ensembl
Outerchr4:76742413..76746661hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg383249
hg193249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11505879, essv11505866, essv11505864, essv11505874, essv11505870, essv11505856, essv11505845, essv11505859, essv11505896, essv11505844, essv11505901, essv11505865, essv11505881, essv11505900, essv11505852, essv11505863, essv11505876, essv11505846, essv11505847, essv11505895, essv11505869, essv11505902, essv11505880, essv11505858, essv11505877, essv11505886, essv11505871, essv11505848, essv11505904, essv11505905, essv11505903, essv11505898, essv11505862, essv11505849, essv11505885, essv11505872, essv11505878, essv11505884, essv11505888, essv11505860, essv11505889, essv11505887, essv11505892, essv11505868, essv11505882, essv11505894, essv11505873, essv11505883, essv11505890, essv11505875, essv11505867, essv11505899, essv11505855, essv11505851, essv11505857, essv11505850, essv11505891, essv11505897, essv11505854, essv11505853, essv11505861, essv11505893
SamplesHG02614, NA18502, HG03484, HG03378, HG02583, NA18917, HG02323, NA19377, HG02888, HG03478, HG03199, NA19446, HG03464, HG03452, NA19457, HG01063, NA19923, HG02315, NA19235, HG03055, NA19451, HG03270, HG02879, HG01139, HG03132, HG02582, HG03291, NA19391, HG01882, HG01879, HG03457, HG02470, HG02757, HG03136, NA18856, NA19099, HG02282, NA19834, HG02983, HG01894, HG02721, NA19835, HG03259, HG03433, HG03473, HG01108, HG03108, HG02558, NA19143, HG03049, HG02938, NA19474, NA19711, HG03470, HG02861, HG02855, NA19463, HG03198, HG02629, HG02643, HG03129, NA19153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601036
Frequency
Sample Size2504
Observed Gain0
Observed Loss62
Observed Complex0
Frequencyn/a


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