A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597143



Internal ID20970214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50041363..50120706hg38UCSC Ensembl
chr22:50479792..50559135hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3879344
hg1979344
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255702
Samples
Known GenesMLC1, MOV10L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597143
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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