A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585461



Internal ID20958532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20465877..20466454hg38UCSC Ensembl
chr14:20934036..20934613hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2036n223
Supporting Variantsnssv18230250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585461
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