A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361976



Internal ID22587645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26586806..26589285hg38UCSC Ensembl
chr11:26608353..26610832hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg382480
hg192480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925217
Supporting Variants
Samples
Known GenesANO3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361976
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.019


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