A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853559



Internal ID22037202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36634302..36634302hg38UCSC Ensembl
chr3:36675794..36675794hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853559
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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