A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196421



Internal ID20763461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66534187..66537713hg38UCSC Ensembl
chr11:66301658..66305184hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383527
hg193527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196421
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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