A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598051



Internal ID20971122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10160887..10161994hg38UCSC Ensembl
chr19:10271563..10272670hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381108
hg191108
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3436n223
Supporting Variantsnssv18244970
Samples
Known GenesDNMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598051
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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