A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586199



Internal ID7057581
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009342
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586199
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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