A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256094



Internal ID21399964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63058456..63264087hg38UCSC Ensembl
chr9:66963428..67219059hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38205632
hg19255632
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730061
Supporting Variants
SamplesNA19238
Known GenesLOC286297
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256094
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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