A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577219



Internal ID20950290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52785500..52785919hg38UCSC Ensembl
chr14:53252218..53252637hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237095
Samples
Known GenesGNPNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577219
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