A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288373



Internal ID20497591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119564526..119569564hg38UCSC Ensembl
chr11:119435237..119440275hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385039
hg195039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747339
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288373
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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