A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460228



Internal ID22518114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22285547..22292073hg38UCSC Ensembl
chr11:22307093..22313619hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg386527
hg196527
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460228
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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