A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268186



Internal ID20477404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23583591..23583656hg38UCSC Ensembl
chr16:23594912..23594977hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746182
Supporting Variants
Samples
Known GenesNDUFAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268186
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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