A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598464



Internal ID6985600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163612678..163686046hg38UCSC Ensembl
Innerchr3:163612678..163686046hg38UCSC Ensembl
Outerchr3:163612178..163686546hg38UCSC Ensembl
chr3:163330466..163403834hg19UCSC Ensembl
Innerchr3:163330466..163403834hg19UCSC Ensembl
Outerchr3:163329966..163404334hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3873369
hg1973369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11213108
SamplesHG03867
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598464
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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