A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086374



Internal ID21995607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2308482..2308482hg38UCSC Ensembl
chr11:2329712..2329712hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590018
Samples
Known GenesTSPAN32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086374
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