A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242819



Internal ID20809859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27948634..27949621hg38UCSC Ensembl
chr16:27959955..27960942hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583007
Supporting Variants
Samples
Known GenesGSG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242819
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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