A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003113



Internal ID7068221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:81085033..81086296hg38UCSC Ensembl
Outerchr16:81118638..81119901hg19UCSC Ensembl
Outerchr16:79676139..79677402hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg381264
hg191264
hg181264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565659
SamplesHuRef
Known GenesGCSH
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003113
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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