A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6294282



Internal ID9271686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184706866..184707377hg38UCSC Ensembl
chr4:185628020..185628531hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667890
Supporting Variants
SamplesNA11918
Known GenesCENPU
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6294282
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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