A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026121



Internal ID21935464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118145908..118149154hg38UCSC Ensembl
chr11:118016623..118019869hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383247
hg193247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604644
Samples
Known GenesSCN4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026121
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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