A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189620



Internal ID20756660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65669164..65686995hg38UCSC Ensembl
chr11:65436635..65454466hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3817832
hg1917832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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