A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094862



Internal ID21479063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13953690..13953690hg38UCSC Ensembl
chr16:14047547..14047547hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650263
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094862
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