A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11063945



Internal ID1065761
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596878
Supporting Variants
SamplesHG03583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11063945
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer