A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189974



Internal ID20757014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108626827..108627643hg38UCSC Ensembl
chr11:108497554..108498370hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189974
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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