A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596920



Internal ID20969991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32430170..32430651hg38UCSC Ensembl
chr19:32921076..32921557hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3495n223
Supporting Variantsnssv18245902
Samples
Known GenesDPY19L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596920
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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