A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596914



Internal ID20969985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34110208..34110817hg38UCSC Ensembl
chr19:34601113..34601722hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246563
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596914
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer