A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564524



Internal ID18765600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:119859648..119859910hg38UCSC Ensembl
Outerchr4:119859634..119859931hg38UCSC Ensembl
Innerchr4:120780803..120781065hg19UCSC Ensembl
Outerchr4:120780789..120781086hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763271
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564524
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