A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532168



Internal ID308096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81643588..81648582hg38UCSC Ensembl
chr16:81677193..81682187hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg384995
hg194995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709859
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532168
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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