A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603565



Internal ID21795612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18211710..18211710hg38UCSC Ensembl
chrUn_gl000212:40462..40462hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383374
hg193374
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603565
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