A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224237



Internal ID20791277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65648301..65675300hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3827000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441548
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224237
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00548


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