A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603450



Internal ID6990481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184013330..184015760hg38UCSC Ensembl
Innerchr4:184013346..184015744hg38UCSC Ensembl
Outerchr4:184013314..184015776hg38UCSC Ensembl
chr4:184934483..184936913hg19UCSC Ensembl
Innerchr4:184934499..184936897hg19UCSC Ensembl
Outerchr4:184934467..184936929hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382431
hg192431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11733307
SamplesHG03476
Known GenesSTOX2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603450
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