A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605632



Internal ID21797679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20936788..20956597hg38UCSC Ensembl
chr16:20948110..20967919hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3819810
hg1919810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024776
Supporting Variants
Samples
Known GenesDNAH3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605632
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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