A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6252190



Internal ID22056800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47328562..47328562hg38UCSC Ensembl
chr22:47724312..47724312hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6252190
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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