A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545180



Internal ID21869535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141599761..141599761hg38UCSC Ensembl
chr3:141318603..141318603hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062039
Supporting Variants
Samples
Known GenesRASA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545180
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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