A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271129



Internal ID20838169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122739451..122740120hg38UCSC Ensembl
chr6:123060596..123061265hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560027
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271129
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