A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263460



Internal ID20472678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63082389..63082389hg38UCSC Ensembl
chr15:63374588..63374588hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38947
hg19947
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750788
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263460
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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