A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548945



Internal ID20922123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135618210..135619026hg38UCSC Ensembl
chr2:136375780..136376596hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255891
Samples
Known GenesR3HDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548945
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