A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225184



Internal ID20792224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41238601..41364900hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38126300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447784
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225184
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.43871


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