A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854099



Internal ID22037742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77698754..77698754hg38UCSC Ensembl
chr3:77747905..77747905hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854099
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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