A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193198



Internal ID20760238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63419201..63430500hg38UCSC Ensembl
chr11:63186673..63197972hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3811300
hg1911300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456753
Supporting Variants
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193198
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.15264


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