A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459059



Internal ID22516941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122536860..122538059hg38UCSC Ensembl
chr11:122407568..122408767hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459059
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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