A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049074



Internal ID20616114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50053901..50054700hg38UCSC Ensembl
chr19:50557158..50557957hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519449
Supporting Variants
Samples
Known GenesFLJ26850
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049074
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