A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614906



Internal ID21806953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30811907..30811907hg38UCSC Ensembl
chr13:31386044..31386044hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614906
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