A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633554



Internal ID21825601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53364858..53364858hg38UCSC Ensembl
chr16:53398770..53398770hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092582
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633554
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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