A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5885563



Internal ID9798458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44017699..44025055hg38UCSC Ensembl
Outerchr4:44017328..44025425hg38UCSC Ensembl
Innerchr4:44019716..44027072hg19UCSC Ensembl
Outerchr4:44019345..44027442hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg388098
hg198098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678664
Supporting Variants
SamplesNA19819
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5885563
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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