A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923613



Internal ID22698840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10215500..10257658hg38UCSC Ensembl
chr11:10237047..10279205hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3842159
hg1942159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363621
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923613
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