A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562909



Internal ID18763985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:171534444..171536247hg38UCSC Ensembl
Outerchr3:171534113..171536541hg38UCSC Ensembl
Innerchr3:171252233..171254036hg19UCSC Ensembl
Outerchr3:171251902..171254330hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg382429
hg192429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761656
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562909
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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