A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854192



Internal ID22037835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:118284589..118284589hg38UCSC Ensembl
chr3:118003436..118003436hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254579
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854192
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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