A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559891



Internal ID332911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20483396..20540345hg38UCSC Ensembl
chr16:20494718..20551667hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3856950
hg1956950
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv197n206
Supporting Variantsnssv17706188
Samples
Known GenesACSM2A, ACSM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559891
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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