A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537492



Internal ID20910826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12328829..12330297hg38UCSC Ensembl
chr1:12388886..12390354hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381469
hg191469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249916
Samples
Known GenesVPS13D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537492
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