A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257328



Internal ID21398498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64773751..64991579hg38UCSC Ensembl
chr9:69786169..70003997hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38217829
hg19217829
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730150
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257328
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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