A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227986



Internal ID20795026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83088301..83099400hg38UCSC Ensembl
chr9:85703216..85714315hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3811100
hg1911100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227986
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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