A curated catalogue of human genomic structural variation




Variant Details

Variant: esv992694



Internal ID6728655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89342073..89342076hg38UCSC Ensembl
chr16:89408481..89408484hg19UCSC Ensembl
chr16:87935982..87935985hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3891
hg1991
hg1891
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3576603
SamplesHuRef
Known GenesANKRD11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv992694
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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