A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084524



Internal ID21993757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23412446..23412446hg38UCSC Ensembl
chr16:23423767..23423767hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg382444
hg192444
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612849
Samples
Known GenesCOG7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084524
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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