A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581505



Internal ID21530005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2940955..2941107hg38UCSC Ensembl
chr4:2942682..2942834hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126019
SamplesHG03125
Known GenesNOP14, NOP14-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581505
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