A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255181



Internal ID22059791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113598010..113598010hg38UCSC Ensembl
chr4:114519166..114519166hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854638
Samples
Known GenesCAMK2D
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255181
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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