A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062633



Internal ID21491612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209771707..209771707hg38UCSC Ensembl
chr1:209945052..209945052hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613320
Supporting Variants
SamplesNA19238
Known GenesTRAF3IP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062633
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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