A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753193



Internal ID20529053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74334515..74334515hg38UCSC Ensembl
chr15:74626856..74626856hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275225
Samples
Known GenesCCDC33
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753193
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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