A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118884



Internal ID21471935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32332477..32332477hg38UCSC Ensembl
chr21:33704786..33704786hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664812
Supporting Variants
SamplesHG03125
Known GenesURB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118884
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