A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474350



Internal ID21131903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89544444..89545241hg38UCSC Ensembl
chr11:89277612..89278409hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996374
Samples
Known GenesNOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474350
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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