A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592570



Internal ID20965641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98714437..98715360hg38UCSC Ensembl
chr13:99366691..99367614hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221439
Samples
Known GenesSLC15A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592570
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