A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006409



Internal ID7071502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:56024093..56026150hg38UCSC Ensembl
Innerchr16:56058005..56060062hg19UCSC Ensembl
Innerchr16:54615506..54617563hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg382058
hg192058
hg182058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587258
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006409
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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