A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533163



Internal ID20906524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63645501..63661900hg38UCSC Ensembl
chr18:61312735..61329134hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3816400
hg1916400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3390n223
Supporting Variantsnssv18177279
Samples
Known GenesSERPINB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533163
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