A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584258



Internal ID20957329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99397484..99398169hg38UCSC Ensembl
chr15:99937689..99938374hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2646n223
Supporting Variantsnssv18239167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584258
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