A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988341



Internal ID20555381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14781667..14784967hg38UCSC Ensembl
chr11:14803213..14806513hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg383301
hg193301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452007
Supporting Variants
Samples
Known GenesPDE3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988341
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