A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596056



Internal ID20969127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41732928..41733529hg38UCSC Ensembl
chr22:42128932..42129533hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255014
Samples
Known GenesMEI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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