A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273771



Internal ID20482989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68777742..68777742hg38UCSC Ensembl
chr18:66444979..66444979hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756731
Supporting Variants
Samples
Known GenesCCDC102B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273771
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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