A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266580



Internal ID20475798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65842795..65843067hg38UCSC Ensembl
chr11:65610266..65610538hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745997
Supporting Variants
Samples
Known GenesSNX32
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266580
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