A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555153



Internal ID20928243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203463190..203464420hg38UCSC Ensembl
chr2:204327913..204329143hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257836
Samples
Known GenesRAPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555153
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