A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6250990



Internal ID22055600
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 StatusM
Merged Variants
Supporting Variantsnssv17848238
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6250990
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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