A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295673



Internal ID20504891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92428626..92428626hg38UCSC Ensembl
chr12:92822402..92822402hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754962
Supporting Variants
Samples
Known GenesCLLU1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295673
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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