A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257259



Internal ID21398365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63423043..64133849hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38710807
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730150
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257259
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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