A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257566



Internal ID21400160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64724183..65025124hg38UCSC Ensembl
chr9:69736601..70010542hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38300942
hg19273942
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730150
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257566
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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