A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528651



Internal ID20902012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45267072..45312498hg38UCSC Ensembl
chr18:42847037..42892463hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3845427
hg1945427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180947
Samples
Known GenesSLC14A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528651
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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