A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578705



Internal ID20951776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102345959..102346481hg38UCSC Ensembl
chr14:102812296..102812818hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578705
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