A curated catalogue of human genomic structural variation




Variant Details

Variant: esv993203



Internal ID6729164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7216639..7222754hg38UCSC Ensembl
Innerchr4:7218366..7224481hg19UCSC Ensembl
Innerchr4:7269267..7275382hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386116
hg196116
hg186116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586434
SamplesHuRef
Known GenesSORCS2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv993203
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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