A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997681



Internal ID7081426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:66278419..66280506hg38UCSC Ensembl
Innerchr2:66505551..66507638hg19UCSC Ensembl
Innerchr2:66359055..66361142hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382088
hg192088
hg182088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv81e180
Supporting Variantsessv3587119
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997681
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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