A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544229



Internal ID20917468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41210451..41210799hg38UCSC Ensembl
chr3:41251942..41252290hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260633
Samples
Known GenesCTNNB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544229
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