A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175862



Internal ID20742902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20384730..20869059hg38UCSC Ensembl
chr9:20384728..20869058hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38484330
hg19484331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420359
Supporting Variants
Samples
Known GenesFOCAD, MIR4473, MIR4474, MIR491, MLLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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