A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618702



Internal ID21810749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68764926..68764926hg38UCSC Ensembl
chr18:66432163..66432163hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109715
Supporting Variants
Samples
Known GenesCCDC102B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618702
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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