A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6251375



Internal ID22055985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30684574..30684574hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6251375
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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