A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269379



Internal ID20836419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151381509..151382509hg38UCSC Ensembl
chr6:151702644..151703644hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564947
Supporting Variants
Samples
Known GenesZBTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269379
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