A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517091



Internal ID293521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66541016..66542349hg38UCSC Ensembl
chr15:66833354..66834687hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704339
Samples
Known GenesZWILCH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517091
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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