A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007819



Internal ID20574860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114134799..114150277hg38UCSC Ensembl
chr13:114900274..114915752hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3815479
hg1915479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007819
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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