A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591237



Internal ID20964308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51686722..51694467hg38UCSC Ensembl
chr15:51978919..51986664hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg387746
hg197746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240343
Samples
Known GenesSCG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591237
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