A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193886



Internal ID20760927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118502169..118560696hg38UCSC Ensembl
chr11:118372884..118431411hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3858528
hg1958528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464913
Supporting Variants
Samples
Known GenesIFT46, KMT2A, TMEM25, TTC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193886
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