A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035967



Internal ID21945310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3096909..3097168hg38UCSC Ensembl
chr11:3118139..3118398hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586649
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035967
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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