A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109817



Internal ID22019050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39327510..39328203hg38UCSC Ensembl
chr7:39367109..39367802hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574796
Samples
Known GenesPOU6F2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109817
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer