A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219231



Internal ID20786271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94252611..94255250hg38UCSC Ensembl
chr9:97014893..97017532hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382640
hg192640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440682
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219231
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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