A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138194



Internal ID21501743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179727828..179727828hg38UCSC Ensembl
chr3:179445616..179445616hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606533
Supporting Variants
SamplesNA19239
Known GenesUSP13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138194
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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