A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597790



Internal ID6984928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131392283..131398294hg38UCSC Ensembl
Innerchr3:131392292..131398285hg38UCSC Ensembl
Outerchr3:131392274..131398303hg38UCSC Ensembl
chr3:131111127..131117138hg19UCSC Ensembl
Innerchr3:131111136..131117129hg19UCSC Ensembl
Outerchr3:131111118..131117147hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg386012
hg196012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11151963
SamplesHG03937
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597790
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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