A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366050



Internal ID22591719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95371605..95372369hg38UCSC Ensembl
chr11:95104769..95105533hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907692
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366050
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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