A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600108



Internal ID6987152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32136832..32346593hg38UCSC Ensembl
Innerchr4:32136832..32346593hg38UCSC Ensembl
Outerchr4:32136332..32347093hg38UCSC Ensembl
chr4:32138454..32348215hg19UCSC Ensembl
Innerchr4:32138454..32348215hg19UCSC Ensembl
Outerchr4:32137954..32348715hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38209762
hg19209762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11388036
SamplesHG01761
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600108
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