A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584406



Internal ID20957477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67265865..67266363hg38UCSC Ensembl
chr14:67732582..67733080hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2184n223
Supporting Variantsnssv18237465
Samples
Known GenesMPP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584406
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