A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129793



Internal ID21439898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179727891..179728038hg38UCSC Ensembl
chr3:179445679..179445826hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569194
Supporting Variants
SamplesHG00732
Known GenesUSP13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129793
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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