A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190999



Internal ID20758039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63642183..63659931hg38UCSC Ensembl
chr18:61309417..61327165hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3817749
hg1917749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534590
Supporting Variants
Samples
Known GenesSERPINB3, SERPINB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190999
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