A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046535



Internal ID20613575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45856562..45860188hg38UCSC Ensembl
chr19:46359820..46363446hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383627
hg193627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533759
Supporting Variants
Samples
Known GenesSYMPK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046535
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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