A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575777



Internal ID20948848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28046817..28047546hg38UCSC Ensembl
chr13:28620954..28621683hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1787n223
Supporting Variantsnssv18223932
Samples
Known GenesFLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575777
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