A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029792



Internal ID20596832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57369253..57379803hg38UCSC Ensembl
chr16:57403165..57413715hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3810551
hg1910551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511329
Supporting Variants
Samples
Known GenesCX3CL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029792
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