A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596130



Internal ID20969201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30934905..31202095hg38UCSC Ensembl
chr22:31330892..31598081hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38267191
hg19267190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255544
Samples
Known GenesINPP5J, MIR3928, MORC2, PLA2G3, RNF185, SELM, SMTN, TUG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596130
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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