A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516885



Internal ID293331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27289481..27291637hg38UCSC Ensembl
chr16:27300802..27302958hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382157
hg192157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706266
Samples
Known GenesFLJ21408
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516885
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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