A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544210



Internal ID21868565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160313056..160313056hg38UCSC Ensembl
chr3:160030844..160030844hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6066570
Supporting Variants
Samples
Known GenesIFT80
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544210
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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