A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467289



Internal ID22525180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32809535..32814694hg38UCSC Ensembl
chr11:32831081..32836240hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385160
hg195160
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866745
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467289
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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