A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518843



Internal ID295209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:33982705..34288052hg38UCSC Ensembl
chr16:33785172..34023150hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38305348
hg19237979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705835
Samples
Known GenesLINC00273
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518843
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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