A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576173



Internal ID20949244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32470130..32471302hg38UCSC Ensembl
chr14:32939336..32940508hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233132
Samples
Known GenesAKAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576173
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