A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763196



Internal ID20539056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39517069..39517069hg38UCSC Ensembl
chr19:40007709..40007709hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382580
hg192580
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287686
Samples
Known GenesSELV
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763196
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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