A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189820



Internal ID20756860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92293985..92381367hg38UCSC Ensembl
chr9:95056267..95143649hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3887383
hg1987383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450674
Supporting Variants
Samples
Known GenesCENPP, NOL8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189820
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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