A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551436



Internal ID21875791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191390411..191390411hg38UCSC Ensembl
chr3:191108200..191108200hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064391
Supporting Variants
Samples
Known GenesCCDC50
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551436
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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