A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271201



Internal ID20838241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33258099..33258880hg38UCSC Ensembl
chr6:33225876..33226657hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574519
Supporting Variants
Samples
Known GenesVPS52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271201
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