A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756731



Internal ID20532591
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 StatusM
Merged Variants
Supporting Variantsnssv16273771
Samples
Known GenesCCDC102B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756731
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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