A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129654



Internal ID21487659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133785382..133785382hg38UCSC Ensembl
chr3:133504226..133504226hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612790
Supporting Variants
SamplesNA18534
Known GenesSRPRB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129654
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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