A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125980



Internal ID21417899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184730507..184730507hg38UCSC Ensembl
chr4:185651661..185651661hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642791
Supporting Variants
SamplesHG00731
Known GenesCENPU
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125980
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