A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674375



Internal ID9940480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151982657..151984820hg38UCSC Ensembl
Outerchr3:151982620..151984870hg38UCSC Ensembl
Innerchr3:151700446..151702609hg19UCSC Ensembl
Outerchr3:151700409..151702659hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382251
hg192251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5809279
SamplesNA20810
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674375
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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