A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256453



Internal ID21398827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18785618..18837333hg38UCSC Ensembl
chr22:18773131..18824846hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3851716
hg1951716
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730176
Supporting Variants
SamplesHG00731
Known GenesGGT3P
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256453
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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