A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080765



Internal ID21989998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54249516..54249516hg38UCSC Ensembl
chr16:54283428..54283428hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080765
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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