A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001250



Internal ID7066378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102918226..102922273hg38UCSC Ensembl
Innerchr14:103384563..103388610hg19UCSC Ensembl
Innerchr14:102454316..102458363hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384048
hg194048
hg184048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587257
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001250
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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