A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241285



Internal ID20808325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71227424..71306452hg38UCSC Ensembl
chr16:71261327..71340355hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3879029
hg1979029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584539
Supporting Variants
Samples
Known GenesCMTR2, HYDIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241285
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