A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449785



Internal ID22507655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89174031..89224669hg38UCSC Ensembl
chr11:88907199..88957837hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3850639
hg1950639
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858165
Supporting Variants
Samples
Known GenesTYR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449785
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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