A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116416



Internal ID21495740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40998439..40998439hg38UCSC Ensembl
chr20:39627079..39627079hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670467
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116416
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