A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5844931



Internal ID8723620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176333786..176334940hg38UCSC Ensembl
Outerchr3:176333752..176334975hg38UCSC Ensembl
Innerchr3:176051574..176052728hg19UCSC Ensembl
Outerchr3:176051540..176052763hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666568
Supporting Variants
SamplesHG00108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5844931
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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