A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540909



Internal ID20914196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26213641..26214947hg38UCSC Ensembl
chr1:26540132..26541438hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381307
hg191307
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540909
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