A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852055



Internal ID22035698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9381652..9381652hg38UCSC Ensembl
chr3:9423336..9423336hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253678
Supporting Variants
Samples
Known GenesTHUMPD3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852055
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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