A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578862



Internal ID20951933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66516160..66516932hg38UCSC Ensembl
chr14:66982878..66983650hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237435
Samples
Known GenesGPHN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578862
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