A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240091



Internal ID20807131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75697464..75787201hg38UCSC Ensembl
chr16:75731362..75821099hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3889738
hg1989738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587961
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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