A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5835036



Internal ID9810678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:59421886..59430113hg38UCSC Ensembl
Outerchr4:59421729..59430266hg38UCSC Ensembl
Innerchr4:60287604..60295831hg19UCSC Ensembl
Outerchr4:60287447..60295984hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg388538
hg198538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661442
Supporting Variants
SamplesNA19916
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5835036
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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