A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598622



Internal ID20971693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30791346..30792322hg38UCSC Ensembl
chr22:31187333..31188309hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4682n223
Supporting Variantsnssv18255535
Samples
Known GenesOSBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598622
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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