A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1656e1



Internal ID6309454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103780705..104057321hg19UCSC Ensembl
chr4:103999805..104276770hg18UCSC Ensembl
chr4:104137960..104414925hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Complex
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsesv93, essv824
SamplesNA18973
Known GenesBDH2, CENPE, CISD2, SLC9B1, SLC9B2, UBE2D3
Method
Analysis
Platform
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)dgv1656e1
Frequency
Sample Size271
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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