A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574092



Internal ID21522504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67230176..67230260hg38UCSC Ensembl
chr4:68095894..68095978hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129905
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574092
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