A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919725



Internal ID22694947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9918290..9919336hg38UCSC Ensembl
chr11:9939837..9940883hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352403
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919725
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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