A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355559



Internal ID22581228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110890649..110890714hg38UCSC Ensembl
chr11:110761373..110761438hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355559
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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