A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160934



Internal ID21475523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136912152..136912152hg38UCSC Ensembl
chr9:139806604..139806604hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637520
Supporting Variants
SamplesHG03486
Known GenesTRAF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160934
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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