A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855918



Internal ID22039561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100847236..100847236hg38UCSC Ensembl
chr4:101768393..101768393hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255057
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855918
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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