A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597881



Internal ID21789925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73316252..73316252hg38UCSC Ensembl
chr15:73608593..73608593hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597881
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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