A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598984



Internal ID20972055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28731143..28731968hg38UCSC Ensembl
chr22:29127131..29127956hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254874
Samples
Known GenesCHEK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598984
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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