A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116411



Internal ID21509249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40969382..40969483hg38UCSC Ensembl
chr20:39598022..39598123hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586752
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116411
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