A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009342



Internal ID7073862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:115474033..115474734hg38UCSC Ensembl
Innerchr1:116016654..116017355hg19UCSC Ensembl
Innerchr1:115818177..115818878hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38702
hg19702
hg18702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586199
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009342
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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