A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587184



Internal ID7058566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61122777..61123306hg38UCSC Ensembl
Innerchr8:62035336..62035865hg19UCSC Ensembl
Innerchr8:62197890..62198419hg18UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38530
hg19530
hg18530
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003680
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587184
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