A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582136



Internal ID21530646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32537906..32538033hg38UCSC Ensembl
chr3:32579398..32579525hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133729
SamplesHG03125
Known GenesDYNC1LI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582136
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