A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557834



Internal ID20930905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113466590..113467340hg38UCSC Ensembl
chr3:113185437..113186187hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259233
Samples
Known GenesSPICE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557834
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