A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283179



Internal ID20492397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15742606..15742606hg38UCSC Ensembl
chr3:15784113..15784113hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764825
Supporting Variants
Samples
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283179
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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