A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145337



Internal ID21421275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10002..32696hg38UCSC Ensembl
chr9:10002..32696hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3822695
hg1922695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668558
Supporting Variants
SamplesHG00731
Known GenesDDX11L5, WASH1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145337
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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