A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008609



Internal ID7058887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:106498214..106499212hg38UCSC Ensembl
Outerchr4:107419371..107420369hg19UCSC Ensembl
Outerchr4:107638820..107639818hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564847
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008609
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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