A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132265



Internal ID21506960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29495161..29495161hg38UCSC Ensembl
chr3:29536652..29536652hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613770
Supporting Variants
SamplesNA19983
Known GenesRBMS3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132265
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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