A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032719



Internal ID20599759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75439738..75466211hg38UCSC Ensembl
chr16:75473636..75500109hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3826474
hg1926474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497295
Supporting Variants
Samples
Known GenesTMEM170A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032719
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