A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047926



Internal ID99816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63250190..63250414hg38UCSC Ensembl
chr11:63017662..63017886hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506993
Supporting Variants
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047926
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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