A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255131



Internal ID22059741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108656486..108656486hg38UCSC Ensembl
chr4:109577642..109577642hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854588
Samples
Known GenesOSTC
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255131
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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