A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526615



Internal ID302740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12828919..12839059hg38UCSC Ensembl
chr16:12922776..12932916hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3810141
hg1910141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707916
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526615
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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