A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595056



Internal ID20968127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72470769..72485963hg38UCSC Ensembl
chr15:72763110..72778304hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3815195
hg1915195
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241880
Samples
Known GenesARIH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595056
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