A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540648



Internal ID20913937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171328163..171328477hg38UCSC Ensembl
chr1:171297302..171297616hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248086
Samples
Known GenesFMO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540648
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