A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559190



Internal ID20932261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151309025..151309151hg38UCSC Ensembl
chr3:151026813..151026939hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263216
Samples
Known GenesGPR87, MED12L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559190
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