A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621423



Internal ID21569728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119796374..119796374hg38UCSC Ensembl
chr4:120717529..120717529hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138417
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621423
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