A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552769



Internal ID21877124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167869726..167869726hg38UCSC Ensembl
chr3:167587514..167587514hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552769
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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