A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521191



Internal ID297487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75892142..75969254hg38UCSC Ensembl
chr16:75926040..76003152hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3877113
hg1977113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521191
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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