A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229721



Internal ID20796761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35972201..35975500hg38UCSC Ensembl
chr9:35972198..35975497hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444733
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00117


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