A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598562



Internal ID6985698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167379219..167382997hg38UCSC Ensembl
Innerchr3:167379228..167382989hg38UCSC Ensembl
Outerchr3:167379211..167383006hg38UCSC Ensembl
chr3:167097007..167100785hg19UCSC Ensembl
Innerchr3:167097016..167100777hg19UCSC Ensembl
Outerchr3:167096999..167100794hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg383779
hg193779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11218895, essv11218894
SamplesHG03086, HG03091
Known GenesZBBX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598562
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer