A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597799



Internal ID20970870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35898438..35899027hg38UCSC Ensembl
chr22:36294486..36295075hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255202
Samples
Known GenesRBFOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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