A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272414



Internal ID20839454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13690985..13691631hg38UCSC Ensembl
chr6:13691217..13691863hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563969
Supporting Variants
Samples
Known GenesRANBP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272414
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer