A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610891



Internal ID21559196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77129512..77129512hg38UCSC Ensembl
chr4:78050665..78050665hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120826
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610891
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