A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256692



Internal ID22061302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116531357..116531357hg38UCSC Ensembl
chr1:117073979..117073979hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17856510
Samples
Known GenesCD58
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256692
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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