A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11190125



Internal ID1191941
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598249
Supporting Variants
SamplesHG04039
Known GenesARHGEF26
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11190125
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