A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592794



Internal ID20965865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31416412..31416520hg38UCSC Ensembl
chr14:31885618..31885726hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226859
Samples
Known GenesHEATR5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592794
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