A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598065



Internal ID6985201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145501960..145538321hg38UCSC Ensembl
Innerchr3:145501987..145538295hg38UCSC Ensembl
Outerchr3:145501934..145538348hg38UCSC Ensembl
chr3:145219747..145256108hg19UCSC Ensembl
Innerchr3:145219774..145256082hg19UCSC Ensembl
Outerchr3:145219721..145256135hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3836362
hg1936362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv945e214
Supporting Variantsessv11170532, essv11170533
SamplesHG00339, HG01432
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598065
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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