A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255695



Internal ID22060305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169657463..169657463hg38UCSC Ensembl
chr4:170578614..170578614hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857065
Samples
Known GenesCLCN3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255695
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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