A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257004



Internal ID21399249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123976823..123997558hg38UCSC Ensembl
chr9:126739102..126759837hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3820736
hg1920736
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730047
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257004
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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