A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258297



Internal ID21400354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123977187..123991074hg38UCSC Ensembl
chr9:126739466..126753353hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3813888
hg1913888
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730047
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258297
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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