A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255406



Internal ID22060016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138129798..138129798hg38UCSC Ensembl
chr4:139050952..139050952hg19UCSC Ensembl
Cytoband4q28.3
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 Variantsnssv17856015
Samples
Known GenesLINC00616, SLC7A11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255406
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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