A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855231



Internal ID22038874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170120773..170120773hg38UCSC Ensembl
chr3:169838561..169838561hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259967
Supporting Variants
Samples
Known GenesPHC3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855231
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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