A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563684



Internal ID336614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74295838..74295889hg38UCSC Ensembl
chr15:74588179..74588230hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg385993
hg195993
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701068
Samples
Known GenesCCDC33
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563684
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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