A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178817



Internal ID20745857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1515505..1923722hg38UCSC Ensembl
chr10:1557700..1965916hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38408218
hg19408217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445708
Supporting Variants
Samples
Known GenesADARB2, ADARB2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178817
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