A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577405



Internal ID20950476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21480828..21481302hg38UCSC Ensembl
chr14:21948987..21949461hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2055n223
Supporting Variantsnssv18231208
Samples
Known GenesTOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577405
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