A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600036



Internal ID21792083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3016284..3016284hg38UCSC Ensembl
chr16:3066285..3066285hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093891
Supporting Variants
Samples
Known GenesCLDN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600036
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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