A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599955



Internal ID6986999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25076711..25085472hg38UCSC Ensembl
Innerchr4:25076711..25085472hg38UCSC Ensembl
Outerchr4:25076211..25085972hg38UCSC Ensembl
chr4:25078333..25087094hg19UCSC Ensembl
Innerchr4:25078333..25087094hg19UCSC Ensembl
Outerchr4:25077833..25087594hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg388762
hg198762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11370926, essv11370925
SamplesHG00306, HG00246
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599955
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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