A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855802



Internal ID22039445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112332178..112332178hg38UCSC Ensembl
chr3:112051025..112051025hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254518
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855802
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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