A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11370924



Internal ID5016858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25054319..25060159hg38UCSC Ensembl
Innerchr4:25054359..25060120hg38UCSC Ensembl
Outerchr4:25054280..25060199hg38UCSC Ensembl
chr4:25055941..25061781hg19UCSC Ensembl
Innerchr4:25055981..25061742hg19UCSC Ensembl
Outerchr4:25055902..25061821hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg385841
hg195841
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599954
Supporting Variants
SamplesNA18510
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11370924
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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