A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255525



Internal ID22060135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152098645..152098645hg38UCSC Ensembl
chr4:153019797..153019797hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854690
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255525
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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