A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591609



Internal ID21540186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76828049..76828103hg38UCSC Ensembl
chr13:77402184..77402238hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081056
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591609
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