A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031440



Internal ID21940783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55847231..55847303hg38UCSC Ensembl
chr16:55881143..55881215hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617547
Samples
Known GenesCES5A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031440
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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