A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574223



Internal ID21522636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165019784..165020033hg38UCSC Ensembl
chr4:165940936..165941185hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129649
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574223
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