A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288276



Internal ID20497494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32208596..32208596hg38UCSC Ensembl
chr5:32208702..32208702hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766711
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288276
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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