A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920856



Internal ID22696079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111722480..111725268hg38UCSC Ensembl
chr11:111593204..111595992hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg382789
hg192789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353160
Samples
Known GenesSIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920856
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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