A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606533



Internal ID21554838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179727828..179727828hg38UCSC Ensembl
chr3:179445616..179445616hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138194, nssv17137320
SamplesNA19238, NA19239
Known GenesUSP13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606533
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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