A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189134



Internal ID20756174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62325417..62389621hg38UCSC Ensembl
chr11:62092889..62157093hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3864205
hg1964205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469898
Supporting Variants
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189134
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0011


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