A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596069



Internal ID20969140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40954051..40954840hg38UCSC Ensembl
chr22:41350055..41350844hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255613
Samples
Known GenesRBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596069
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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