A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031692



Internal ID20598732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68252899..68256272hg38UCSC Ensembl
chr16:68286802..68290175hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383374
hg193374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510278
Supporting Variants
Samples
Known GenesPLA2G15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031692
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