A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596878



Internal ID6637148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86899036..86905821hg38UCSC Ensembl
Innerchr3:86899036..86905821hg38UCSC Ensembl
Outerchr3:86898803..86906035hg38UCSC Ensembl
chr3:86948186..86954971hg19UCSC Ensembl
Innerchr3:86948186..86954971hg19UCSC Ensembl
Outerchr3:86947953..86955185hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg386786
hg196786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11063945, essv11063946, essv11063944
SamplesHG03095, HG03583, NA18984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596878
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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