A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528669



Internal ID304716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63459776..63459835hg38UCSC Ensembl
chr15:63751975..63752034hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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