A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189537



Internal ID20756577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69774515..69785523hg38UCSC Ensembl
chr15:70066854..70077862hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3811009
hg1911009
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513655
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189537
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