A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560973



Internal ID21885328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151534970..151534970hg38UCSC Ensembl
chr5:150914531..150914531hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079675
Supporting Variants
Samples
Known GenesFAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560973
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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