A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848238



Internal ID22031881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30661856..30661856hg38UCSC Ensembl
chr19:31152763..31152763hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6250990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848238
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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