A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531834



Internal ID307778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54409591..54410599hg38UCSC Ensembl
chr16:54443503..54444511hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531834
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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