A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097968



Internal ID22007201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52556492..52556492hg38UCSC Ensembl
chr16:52590404..52590404hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627100
Samples
Known GenesCASC16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097968
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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