A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257449



Internal ID21398158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75206041..75222884hg38UCSC Ensembl
chr16:75239939..75256782hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3816844
hg1916844
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730054
Supporting Variants
SamplesHG00513
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257449
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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