A curated catalogue of human genomic structural variation




Variant Details

Variant: esv993809



Internal ID7078800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:141805170..141814245hg38UCSC Ensembl
Outerchr5:141184737..141193810hg19UCSC Ensembl
Outerchr5:141164921..141173994hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg389076
hg199074
hg189074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563519
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv993809
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