A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290656



Internal ID20499874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43323460..43323460hg38UCSC Ensembl
chr20:41952100..41952100hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755664
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290656
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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