A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242786



Internal ID22047396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9582886..9582886hg38UCSC Ensembl
chr19:9693562..9693562hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17849596
Samples
Known GenesZNF121
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242786
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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