A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767088



Internal ID20542948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75204667..75224295hg38UCSC Ensembl
chr16:75238565..75258193hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3819629
hg1919629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv43n199
Supporting Variantsnssv16290320
Samples
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767088
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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