A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597212



Internal ID20970283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36091476..36092161hg38UCSC Ensembl
chr22:36487524..36488209hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597212
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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