A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231898



Internal ID20798938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64016801..64134700hg38UCSC Ensembl
chrUn_gl000211:48354..166253hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38117900
hg19117900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439380
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00367


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