A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283096



Internal ID20492314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69220532..69220532hg38UCSC Ensembl
chr4:70086250..70086250hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg382876
hg192876
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767624
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283096
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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