A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994831



Internal ID6730781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89429172..89429885hg38UCSC Ensembl
chr16:89495580..89496293hg19UCSC Ensembl
chr16:88023081..88023794hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38714
hg19714
hg18714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3566841
SamplesHuRef
Known GenesANKRD11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994831
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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