A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029663



Internal ID20596703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4627539..4628138hg38UCSC Ensembl
chr16:4677540..4678139hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496802
Supporting Variants
Samples
Known GenesMGRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00968


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