A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538563



Internal ID20911877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222690413..222691218hg38UCSC Ensembl
chr2:223555132..223555937hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259409
Samples
Known GenesMOGAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538563
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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