A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3564419



Internal ID18765495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108186534..108186811hg38UCSC Ensembl
Outerchr4:108186475..108186874hg38UCSC Ensembl
Innerchr4:109107690..109107967hg19UCSC Ensembl
Outerchr4:109107631..109108030hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9763166
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3564419
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