A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257345



Internal ID21398910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123976373..123993780hg38UCSC Ensembl
chr9:126738652..126756059hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3817408
hg1917408
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730047
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257345
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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