A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150203



Internal ID21468536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107794146..107794146hg38UCSC Ensembl
chr9:110556427..110556427hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632637
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150203
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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