A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6015n223



Internal ID22808983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164452003..164452789hg38UCSC Ensembl
chr5:163879009..163879795hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6572867, nsv6561418
Samples
Known GenesLOC101927835
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6015n223
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