A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092312



Internal ID21487786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20860639..20860639hg38UCSC Ensembl
chr13:21434778..21434778hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660039
Supporting Variants
SamplesNA18534
Known GenesXPO4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092312
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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