A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991169



Internal ID20558209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47737057..47742764hg38UCSC Ensembl
chr11:47758609..47764316hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385708
hg195708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459415
Supporting Variants
Samples
Known GenesFNBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991169
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