A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553464



Internal ID20926573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218446480..218448777hg38UCSC Ensembl
chr2:219311203..219313500hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382298
hg192298
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4283n223
Supporting Variantsnssv18259337
Samples
Known GenesVIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553464
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