A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079672



Internal ID21988905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:510816..510816hg38UCSC Ensembl
chr7:550453..550453hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564673
Samples
Known GenesPDGFA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079672
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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