A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223199



Internal ID20790239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65703901..65718500hg38UCSC Ensembl
chr9:42684821..42699420hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814600
hg1914600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442056
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00095


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