A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271175



Internal ID20480393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107590333..107590405hg38UCSC Ensembl
chr11:107461059..107461131hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743301
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271175
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