A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124143



Internal ID21510932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141599751..141599751hg38UCSC Ensembl
chr3:141318593..141318593hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612052
Supporting Variants
SamplesNA24385
Known GenesRASA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124143
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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