A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116207



Internal ID21446352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2659082..2659082hg38UCSC Ensembl
chr20:2639728..2639728hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648112
Supporting Variants
SamplesHG00732
Known GenesIDH3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116207
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