A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229167



Internal ID20796207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21558501..21560900hg38UCSC Ensembl
chr9:21558500..21560899hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435023
Supporting Variants
Samples
Known GenesMIR31HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229167
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