A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135013



Internal ID21448147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111055365..111055365hg38UCSC Ensembl
chr5:110391063..110391063hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626085
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135013
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