A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450519



Internal ID21108072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105491385..105494387hg38UCSC Ensembl
chr9:108253666..108256668hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg383003
hg193003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172360
Samples
Known GenesFSD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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