A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267892



Internal ID20477110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71158079..71158079hg38UCSC Ensembl
chr3:71207230..71207230hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766801
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267892
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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