A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749264



Internal ID20525294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45111211..45111405hg38UCSC Ensembl
chr11:45132762..45132956hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275026
Samples
Known GenesPRDM11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749264
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer