A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17856600



Internal ID22040243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158967746..158967746hg38UCSC Ensembl
chr3:158685535..158685535hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17856600
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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