A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612790



Internal ID21804837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99427145..99427145hg38UCSC Ensembl
chr13:100079399..100079399hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084767
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612790
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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