A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256453



Internal ID22061063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169163831..169163831hg38UCSC Ensembl
chr5:168590835..168590835hg19UCSC Ensembl
Cytoband5q35.1
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 Variantsnssv17858850
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256453
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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