A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115885



Internal ID21446169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19003194..19003275hg38UCSC Ensembl
chr20:18983838..18983919hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598851
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115885
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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