A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909886



Internal ID22685096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93327758..93332031hg38UCSC Ensembl
chr11:93060924..93065197hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384274
hg194274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363710
Samples
Known GenesCCDC67
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909886
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