A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549263



Internal ID21873618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15069386..15069386hg38UCSC Ensembl
chr3:15110893..15110893hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549263
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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