A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256335



Internal ID22060945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157855192..157855192hg38UCSC Ensembl
chr5:157282200..157282200hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858644
Samples
Known GenesCLINT1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256335
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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