A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292469



Internal ID20501687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73112346..73112346hg38UCSC Ensembl
chr10:74872104..74872104hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756674
Supporting Variants
Samples
Known GenesNUDT13
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292469
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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