A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530755



Internal ID306727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100198183..100600807hg38UCSC Ensembl
chr15:100738388..101141012hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38402625
hg19402625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703830
Samples
Known GenesADAMTS17, CERS3, LINS, PRKXP1, SPATA41
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530755
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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