A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243622



Internal ID20810663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67607034..67608184hg38UCSC Ensembl
chr16:67640937..67642087hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381151
hg191151
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586159
Supporting Variants
Samples
Known GenesCTCF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243622
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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