A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1011253



Internal ID6723341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89299921..89303507hg38UCSC Ensembl
Outerchr16:89366329..89369915hg19UCSC Ensembl
Outerchr16:87893830..87897416hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg383587
hg193587
hg183587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564323
SamplesHuRef
Known GenesANKRD11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1011253
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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