A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999768



Internal ID7082376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129054349..129055969hg38UCSC Ensembl
Innerchr10:130852613..130854233hg19UCSC Ensembl
Innerchr10:130742603..130744223hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381621
hg191621
hg181621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586469
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999768
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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