A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190914



Internal ID20757954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113381536..113511534hg38UCSC Ensembl
chr13:114035851..114165849hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38129999
hg19129999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488962
Supporting Variants
Samples
Known GenesADPRHL1, DCUN1D2, TMCO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190914
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