A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023564



Internal ID21932907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84797471..84899016hg38UCSC Ensembl
chr16:84831077..84932622hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38101546
hg19101546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621512
Samples
Known GenesCRISPLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023564
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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