A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595972



Internal ID20969043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32704415..32705002hg38UCSC Ensembl
chr19:33195321..33195908hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245909
Samples
Known GenesNUDT19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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