A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596863



Internal ID20969934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16243275..16243950hg38UCSC Ensembl
chr19:16354086..16354761hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596863
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