A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989714



Internal ID20556754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31799101..31799500hg38UCSC Ensembl
chr11:31820649..31821048hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437411
Supporting Variants
Samples
Known GenesPAX6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03702


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