A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245961



Internal ID20813001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57201189..57201926hg38UCSC Ensembl
chr17:55278550..55279287hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583399
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245961
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