A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552689



Internal ID20925815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33554128..33556566hg38UCSC Ensembl
chr3:33595620..33598058hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg382439
hg192439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262056
Samples
Known GenesCLASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552689
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