A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555694



Internal ID21880049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160312941..160312941hg38UCSC Ensembl
chr3:160030729..160030729hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072710
Supporting Variants
Samples
Known GenesIFT80
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555694
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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