A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840718



Internal ID22024361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113715592..113715592hg38UCSC Ensembl
chr8:114727821..114727821hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246530
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17840718
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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