A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538268



Internal ID20911589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35769642..35770141hg38UCSC Ensembl
chr22:36165689..36166188hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074222
Samples
Known GenesRBFOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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