A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756786



Internal ID20532646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48616906..48616972hg38UCSC Ensembl
chr16:48650817..48650883hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756786
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer