A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854955



Internal ID22629890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22285547..22292073hg38UCSC Ensembl
chr11:22307093..22313619hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg386527
hg196527
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854955
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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