A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11542063



Internal ID1543879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98876811..98879628hg38UCSC Ensembl
Innerchr4:98876811..98879628hg38UCSC Ensembl
Outerchr4:98876780..98879686hg38UCSC Ensembl
chr4:99797962..99800779hg19UCSC Ensembl
Innerchr4:99797962..99800779hg19UCSC Ensembl
Outerchr4:99797931..99800837hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382818
hg192818
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601546
Supporting Variants
SamplesHG02491
Known GenesEIF4E
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11542063
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