A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159873



Internal ID21427531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121879722..121879854hg38UCSC Ensembl
chr9:124642001..124642133hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590354
Supporting Variants
SamplesHG00731
Known GenesTTLL11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159873
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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