A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598873



Internal ID20971944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10160879..10162142hg38UCSC Ensembl
chr19:10271555..10272818hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3436n223
Supporting Variantsnssv18244969
Samples
Known GenesDNMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598873
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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