A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754720



Internal ID20530580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77133041..77285957hg38UCSC Ensembl
chr16:77166938..77319854hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38152917
hg19152917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv44n199
Supporting Variantsnssv16258902
Samples
Known GenesADAMTS18, MON1B, SYCE1L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754720
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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