A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196665



Internal ID20763705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65960669..65967340hg38UCSC Ensembl
chr11:65728140..65734811hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg386672
hg196672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457887
Supporting Variants
Samples
Known GenesSART1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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