A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185598



Internal ID20752638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23392901..23413700hg38UCSC Ensembl
chr11:23414447..23435246hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3820800
hg1920800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437460
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00048


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