A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194498



Internal ID20761538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1685001..1693200hg38UCSC Ensembl
chr11:1706231..1714430hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453107
Supporting Variants
Samples
Known GenesFAM99B, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194498
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