A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581683



Internal ID20954754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57299949..57300563hg38UCSC Ensembl
chr16:57333861..57334475hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239322
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581683
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