A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223766



Internal ID20790806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63542501..63563000hg38UCSC Ensembl
chr9:68138235..68158734hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3820500
hg1920500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445913
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223766
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00033


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