A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220454



Internal ID20787494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66252301..66269700hg38UCSC Ensembl
chr9:42251943..42268712hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3817400
hg1916770
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451448
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220454
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00136


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