A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854017



Internal ID22037660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217075602..217075602hg38UCSC Ensembl
chr2:217940325..217940325hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854017
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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