A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226138



Internal ID20793178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98789501..98815900hg38UCSC Ensembl
chr9:101551783..101578182hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3826400
hg1926400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439111
Supporting Variants
Samples
Known GenesANKS6, GALNT12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226138
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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