A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004883



Internal ID6717006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14954811..15028937hg38UCSC Ensembl
Innerchr16:15048668..15122794hg19UCSC Ensembl
Innerchr16:14956169..15030295hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3874127
hg1974127
hg1874127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586157
SamplesHuRef
Known GenesMIR1972-1, MIR1972-2, PDXDC1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004883
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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