A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620596



Internal ID21568901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:315827..315827hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3865
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167170, nssv17167169
SamplesHG03125, NA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620596
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer