A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189549



Internal ID20756589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5862301..5928000hg38UCSC Ensembl
chr11:5883531..5949230hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3865700
hg1965700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444268
Supporting Variants
Samples
Known GenesOR52E4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189549
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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