A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031110



Internal ID21940453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89186707..89187027hg38UCSC Ensembl
chr16:89253115..89253435hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621311
Samples
Known GenesCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031110
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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