A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599441



Internal ID20972512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12849592..12850102hg38UCSC Ensembl
chr19:12960406..12960916hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3446n223
Supporting Variantsnssv18245080
Samples
Known GenesMAST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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