A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515186



Internal ID291672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66381862..66384711hg38UCSC Ensembl
chr15:66674200..66677049hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382850
hg192850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515186
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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