A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106124



Internal ID22015357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75204667..75222749hg38UCSC Ensembl
chr16:75238565..75256647hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3818083
hg1918083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634626
Samples
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106124
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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