A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255521



Internal ID22060131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151910400..151910400hg38UCSC Ensembl
chr4:152831552..152831552hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255521
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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