A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632729



Internal ID21824776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84870953..84935891hg38UCSC Ensembl
chr16:84904559..84969497hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3864939
hg1964939
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034217
Supporting Variants
Samples
Known GenesCRISPLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632729
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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