A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596868



Internal ID6984182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86573595..86574985hg38UCSC Ensembl
Innerchr3:86573595..86574985hg38UCSC Ensembl
Outerchr3:86573065..86575198hg38UCSC Ensembl
chr3:86622745..86624135hg19UCSC Ensembl
Innerchr3:86622745..86624135hg19UCSC Ensembl
Outerchr3:86622215..86624348hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11063797, essv11063810, essv11063782, essv11063792, essv11063791, essv11063800, essv11063784, essv11063807, essv11063801, essv11063794, essv11063781, essv11063803, essv11063795, essv11063780, essv11063814, essv11063790, essv11063789, essv11063787, essv11063796, essv11063805, essv11063804, essv11063798, essv11063802, essv11063812, essv11063808, essv11063809, essv11063793, essv11063786, essv11063785, essv11063783, essv11063788, essv11063799, essv11063806, essv11063813, essv11063811
SamplesNA19399, NA19446, HG03572, NA19374, HG03464, HG03091, HG03460, HG03556, HG03189, NA19317, HG02623, NA20127, HG03270, HG02716, NA19984, NA19043, HG01989, HG03136, HG03476, NA19031, HG01241, NA19257, NA19160, HG02282, NA19108, HG03437, NA19019, NA19473, NA19144, NA19328, HG03279, HG02053, NA19474, HG02768, NA19146
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596868
Frequency
Sample Size2504
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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