A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598469



Internal ID6985605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163784000..163816493hg38UCSC Ensembl
Innerchr3:163784000..163816493hg38UCSC Ensembl
Outerchr3:163783500..163816993hg38UCSC Ensembl
chr3:163501788..163534281hg19UCSC Ensembl
Innerchr3:163501788..163534281hg19UCSC Ensembl
Outerchr3:163501288..163534781hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3832494
hg1932494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11213120
SamplesHG03856
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598469
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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