A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587329



Internal ID21535888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3961125..3961630hg38UCSC Ensembl
chr11:3982355..3982860hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074936
SamplesNA19239
Known GenesSTIM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587329
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