A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11359086



Internal ID3206071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12705628..12733130hg38UCSC Ensembl
Innerchr4:12705640..12733119hg38UCSC Ensembl
Outerchr4:12705617..12733142hg38UCSC Ensembl
chr4:12707252..12734754hg19UCSC Ensembl
Innerchr4:12707264..12734743hg19UCSC Ensembl
Outerchr4:12707241..12734766hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3827503
hg1927503
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599687
Supporting Variants
SamplesHG02813
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11359086
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer