A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367747



Internal ID22593416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102242732..102249692hg38UCSC Ensembl
chr11:102113463..102120423hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg386961
hg196961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925884
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367747
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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