A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003652



Internal ID7068757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136302203..136307356hg38UCSC Ensembl
Innerchr3:136021045..136026198hg19UCSC Ensembl
Innerchr3:137503735..137508888hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385154
hg195154
hg185154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586318
SamplesHuRef
Known GenesPCCB
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003652
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