A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242476



Internal ID22047086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54908055..54908055hg38UCSC Ensembl
chr18:52575286..52575286hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17847471
Samples
Known GenesCCDC68
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242476
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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