A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579353



Internal ID21527832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44034101..44034275hg38UCSC Ensembl
chr3:44075593..44075767hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124830
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579353
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