A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224991



Internal ID20792031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41238501..41421600hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38183100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442006
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.38402


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