A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598455



Internal ID6985591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163383490..163472977hg38UCSC Ensembl
Innerchr3:163383490..163472977hg38UCSC Ensembl
Outerchr3:163382990..163473477hg38UCSC Ensembl
chr3:163101278..163190765hg19UCSC Ensembl
Innerchr3:163101278..163190765hg19UCSC Ensembl
Outerchr3:163100778..163191265hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3889488
hg1989488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11213089
SamplesHG02666
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598455
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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