A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177465



Internal ID20744505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90077401..90178800hg38UCSC Ensembl
chr11:89810569..89911968hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38101400
hg19101400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459895
Supporting Variants
Samples
Known GenesNAALAD2, UBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177465
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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