A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580725



Internal ID21529218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162936494..162936544hg38UCSC Ensembl
chr1:162906284..162906334hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061496
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580725
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