A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581970



Internal ID21530476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43264795..43272510hg38UCSC Ensembl
chr4:43266812..43274527hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg387716
hg197716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135175
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581970
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