A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105984



Internal ID22015217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68777730..68777730hg38UCSC Ensembl
chr18:66444967..66444967hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633438
Samples
Known GenesCCDC102B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105984
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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