A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180903



Internal ID20747943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87059401..87068100hg38UCSC Ensembl
chr9:89674316..89683015hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00117


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