A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256241



Internal ID21400768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64370483..65048344hg38UCSC Ensembl
chr9:69382901..70010542hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38677862
hg19627642
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730150
Supporting Variants
SamplesNA19240
Known GenesANKRD20A4, LOC100133920
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256241
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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