A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762761



Internal ID20538621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42743581..42743581hg38UCSC Ensembl
chr3:42785073..42785073hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272072
Samples
Known GenesCCDC13, CCDC13-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762761
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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