A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357418



Internal ID22583087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69482419..69482498hg38UCSC Ensembl
chr11:69297187..69297266hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917809
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357418
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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