A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029635



Internal ID21938978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65970747..65971631hg38UCSC Ensembl
chr11:65738218..65739102hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582185
Samples
Known GenesSART1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029635
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