A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560072



Internal ID20933143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133679397..133679484hg38UCSC Ensembl
chr3:133398241..133398328hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560072
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