A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624067



Internal ID21816114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1150053..1150053hg38UCSC Ensembl
chr20:1130696..1130696hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108417
Supporting Variants
Samples
Known GenesPSMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624067
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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