A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032316



Internal ID21941659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65970788..65970856hg38UCSC Ensembl
chr11:65738259..65738327hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586643
Samples
Known GenesSART1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032316
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