A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565620



Internal ID7037002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:75786384..75787099hg38UCSC Ensembl
Outerchr5:75082209..75082924hg19UCSC Ensembl
Outerchr5:75117965..75118680hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38716
hg19716
hg18716
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988051
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565620
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