A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030847



Internal ID20597887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67934601..67936900hg38UCSC Ensembl
chr16:67968504..67970803hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502077
Supporting Variants
Samples
Known GenesPSMB10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030847
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