A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256451



Internal ID22061061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169035629..169035629hg38UCSC Ensembl
chr5:168462634..168462634hg19UCSC Ensembl
Cytoband5q34
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 Variantsnssv17858848
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256451
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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