A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545098



Internal ID21869453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91663234..91663234hg38UCSC Ensembl
chr5:90959051..90959051hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545098
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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