A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184687



Internal ID20751727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86790474..86796634hg38UCSC Ensembl
chr9:89405389..89411549hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386161
hg196161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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