A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562522



Internal ID18763598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128661953..128683946hg38UCSC Ensembl
Outerchr3:128656658..128685223hg38UCSC Ensembl
Innerchr3:128380796..128402789hg19UCSC Ensembl
Outerchr3:128375501..128404066hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3828566
hg1928566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761269
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562522
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