A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005806



Internal ID6717926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:13200105..13202692hg38UCSC Ensembl
Outerchr16:13293962..13296549hg19UCSC Ensembl
Outerchr16:13201463..13204050hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg382588
hg192588
hg182588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563558
SamplesHuRef
Known GenesSHISA9
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005806
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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