A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190961



Internal ID20758001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3467317..3470018hg38UCSC Ensembl
chr9:3467317..3470018hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416037
Supporting Variants
Samples
Known GenesRFX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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