A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598249



Internal ID6638514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154166561..154180276hg38UCSC Ensembl
Innerchr3:154166561..154180276hg38UCSC Ensembl
Outerchr3:154166061..154180776hg38UCSC Ensembl
chr3:153884350..153898065hg19UCSC Ensembl
Innerchr3:153884350..153898065hg19UCSC Ensembl
Outerchr3:153883850..153898565hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3813716
hg1913716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11190125
SamplesHG04039
Known GenesARHGEF26
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598249
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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