A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602621



Internal ID21794668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131918793..131918793hg38UCSC Ensembl
chr12:132403338..132403338hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083559
Supporting Variants
Samples
Known GenesULK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602621
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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