A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5909n223



Internal ID22808877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117831178..117831824hg38UCSC Ensembl
chr5:117166873..117167519hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6567533, nsv6571118
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5909n223
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