A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222491



Internal ID20789531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81842469..81869946hg38UCSC Ensembl
chr9:84457384..84484861hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3827478
hg1927478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445312
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222491
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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