A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29952



Internal ID11394161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32040151..33829114hg38UCSC Ensembl
Innerchr16:32051472..33631581hg19UCSC Ensembl
Innerchr16:31958973..33539082hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381788964
hg191580110
hg181580110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84191
SamplesWATSON
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodOligo aCGH
AnalysisThe data were analyzed using the CGH Analytics software.
PlatformAgilent-014584 Human Genome 244K CGH Microarray (Alpha Test)
Comments
ReferenceWheeler_et_al_2008
Pubmed ID18421352
Accession Number(s)esv29952
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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