A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275471



Internal ID20484689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6069990..6070904hg38UCSC Ensembl
chr19:6070001..6070915hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744515
Supporting Variants
Samples
Known GenesRFX2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275471
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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