A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921064



Internal ID22696287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90075126..90114362hg38UCSC Ensembl
chr11:89808294..89847530hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3839237
hg1939237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359257
Samples
Known GenesUBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921064
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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