A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001550



Internal ID7066674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87153264..87157415hg38UCSC Ensembl
Innerchr4:88074416..88078567hg19UCSC Ensembl
Innerchr4:88293440..88297591hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg384152
hg194152
hg184152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586276
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001550
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