A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517768



Internal ID294181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60100000..60118937hg38UCSC Ensembl
chr15:60392199..60411136hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3818938
hg1918938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517768
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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