A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255291



Internal ID22059901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125225639..125225639hg38UCSC Ensembl
chr4:126146794..126146794hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255291
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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