A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599966



Internal ID6987010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25500074..25507383hg38UCSC Ensembl
Innerchr4:25500086..25507372hg38UCSC Ensembl
Outerchr4:25500063..25507395hg38UCSC Ensembl
chr4:25501696..25509005hg19UCSC Ensembl
Innerchr4:25501708..25508994hg19UCSC Ensembl
Outerchr4:25501685..25509017hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg387310
hg197310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11373296, essv11373294, essv11373295, essv11373297, essv11373299, essv11373298
SamplesHG01986, HG01985, HG03078, HG03024, NA19223, HG03097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599966
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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