A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122216



Internal ID21500445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153222046..153222046hg38UCSC Ensembl
chr4:154143198..154143198hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622189
Supporting Variants
SamplesNA19239
Known GenesTRIM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122216
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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