A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11373296



Internal ID3374273
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599966
Supporting Variants
SamplesHG03024
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11373296
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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