A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544728



Internal ID21869083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11566..11566hg38UCSC Ensembl
chr5:11566..11566hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544728
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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