A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241301



Internal ID20808341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71809129..71813512hg38UCSC Ensembl
chr16:71843032..71847415hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg384384
hg194384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241301
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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