A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616763



Internal ID21565068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179723569..179723569hg38UCSC Ensembl
chr3:179441357..179441357hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138975
SamplesHG03732
Known GenesUSP13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616763
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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