A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532241



Internal ID308169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81683483..81683855hg38UCSC Ensembl
chr16:81717088..81717460hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709863
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532241
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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