A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240649



Internal ID20807689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46771511..46773041hg38UCSC Ensembl
chr16:46805423..46806953hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg381531
hg191531
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240649
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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