A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598261



Internal ID6985397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154872797..154875103hg38UCSC Ensembl
Innerchr3:154872833..154875068hg38UCSC Ensembl
Outerchr3:154872762..154875139hg38UCSC Ensembl
chr3:154590586..154592892hg19UCSC Ensembl
Innerchr3:154590622..154592857hg19UCSC Ensembl
Outerchr3:154590551..154592928hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg382307
hg192307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11190158
SamplesHG01669
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598261
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