A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576168



Internal ID20949239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23669708..23670708hg38UCSC Ensembl
chr14:24138917..24139917hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576168
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