A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595985



Internal ID20969056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27090125..27381939hg38UCSC Ensembl
chr22:27486087..27777900hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38291815
hg19291814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595985
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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