A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181753



Internal ID20748793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113482740..113529446hg38UCSC Ensembl
chr13:114137055..114183761hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3846707
hg1946707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492448
Supporting Variants
Samples
Known GenesDCUN1D2, TMCO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181753
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