A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647014



Internal ID7033756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39103596..39107710hg38UCSC Ensembl
Innerchr21:39103597..39107710hg38UCSC Ensembl
Outerchr21:39103596..39107711hg38UCSC Ensembl
chr21:40475522..40479636hg19UCSC Ensembl
Innerchr21:40475523..40479636hg19UCSC Ensembl
Outerchr21:40475522..40479637hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg384115
hg194115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16320795, essv16320839, essv16320806, essv16320800, essv16320836, essv16320832, essv16320790, essv16320809, essv16320823, essv16320808, essv16320789, essv16320803, essv16320791, essv16320833, essv16320805, essv16320793, essv16320819, essv16320810, essv16320816, essv16320828, essv16320826, essv16320804, essv16320814, essv16320820, essv16320798, essv16320821, essv16320824, essv16320799, essv16320827, essv16320838, essv16320792, essv16320812, essv16320825, essv16320813, essv16320834, essv16320811, essv16320801, essv16320822, essv16320794, essv16320837, essv16320829, essv16320831, essv16320818, essv16320796, essv16320797, essv16320807, essv16320815, essv16320817, essv16320802, essv16320830, essv16320835
SamplesHG03800, NA20877, NA12286, HG03960, HG04076, HG03941, HG03926, HG03229, NA20864, NA20863, NA21128, HG03999, NA20894, NA19746, HG02312, NA21135, NA20796, HG01766, HG03873, NA20795, HG04185, HG03750, NA20587, HG04029, NA21122, HG00108, HG01524, HG03908, NA20809, NA20810, NA21118, HG03919, HG02221, HG04235, HG03951, HG02332, HG00246, NA20799, NA21144, NA12272, HG02685, NA20868, HG02238, HG03849, NA21102, NA21133, HG01269, HG01781, HG04056, HG03815, NA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647014
Frequency
Sample Size2504
Observed Gain0
Observed Loss51
Observed Complex0
Frequencyn/a


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