A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567874



Internal ID21516215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:90204389..90205371hg38UCSC Ensembl
chr3:90253539..90254521hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38983
hg19983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138821
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567874
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